Human (GRCh38.p14)
Description

ninein [Source:HGNC Symbol;Acc:HGNC:14906]

Location
About this transcript

This transcript has 31 exons, is annotated with 46 domains and features, is associated with 49280 variant alleles and maps to 1236 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000530997.7NIN-215103342133aaENSP00000436092.2
 
Protein coding
CCDS91876Q8N4C6-7 NM_020921.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P2TSL:5
ENST00000476352.5NIN-209102251989aaENSP00000432924.1
 
Protein coding
E9PN67 -GENCODE basicAPPRIS ALT2TSL:5
ENST00000706706.1NIN-22580891235aaENSP00000516509.1
 
Protein coding
--GENCODE basicAPPRIS ALT2
ENST00000453196.6NIN-20568582046aaENSP00000412391.1
 
Protein coding
CCDS45103C9J066 -GENCODE basicAPPRIS ALT2TSL:5
ENST00000382041.7NIN-20264962090aaENSP00000371472.3
 
Protein coding
CCDS32079Q8N4C6-1 -GENCODE basicAPPRIS ALT2TSL:1
ENST00000389869.7NIN-20447881581aaENSP00000374519.3
 
Protein coding
H9KV85 -TSL:5CDS 5' incomplete
ENST00000485005.2NIN-21146011238aaENSP00000431485.2
 
Protein coding
A0A0B4J215 -GENCODE basicAPPRIS ALT2TSL:1
ENST00000324330.13NIN-20143641377aaENSP00000324210.10
 
Protein coding
CCDS32078Q8N4C6-11 -GENCODE basicAPPRIS ALT2TSL:5
ENST00000382043.8NIN-20342161377aaENSP00000371474.4
 
Protein coding
CCDS32078Q8N4C6-11 -GENCODE basicAPPRIS ALT2TSL:1
ENST00000453401.6NIN-2061418396aaENSP00000398641.2
 
Protein coding
H7C162 -TSL:1CDS 3' incomplete
ENST00000486950.5NIN-213605116aaENSP00000473530.1
 
Protein coding
R4GN85 -TSL:3CDS 5' incomplete
ENST00000496749.1NIN-214569101aaENSP00000431826.1
 
Protein coding
E9PJH9 -TSL:4CDS 3' incomplete
ENST00000674061.1NIN-221342114aaENSP00000501163.1
 
Protein coding
A0A669KBB6 -CDS 5' and 3' incomplete
ENST00000674030.1NIN-2208290597aaENSP00000501260.1
 
Nonsense mediated decay
A0A669KBI5 --
ENST00000673657.1NIN-2178106373aaENSP00000501199.1
 
Nonsense mediated decay
A0A669KBE5 --
ENST00000706705.1NIN-2247901644aaENSP00000516508.1
 
Nonsense mediated decay
---
ENST00000673852.1NIN-21932131aaENSP00000501307.1
 
Nonsense mediated decay
A0A669KBK6 -CDS 5' incomplete
ENST00000673819.1NIN-2181287No protein-
 
Protein coding CDS not defined
---
ENST00000486200.1NIN-212465No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000706704.1NIN-2236268No protein-
 
Retained intron
---
ENST00000706709.1NIN-2285671No protein-
 
Retained intron
---
ENST00000706707.1NIN-2264867No protein-
 
Retained intron
---
ENST00000706703.1NIN-2224554No protein-
 
Retained intron
---
ENST00000706708.1NIN-2273674No protein-
 
Retained intron
---
ENST00000706711.1NIN-2303204No protein-
 
Retained intron
---
ENST00000706712.1NIN-2312979No protein-
 
Retained intron
---
ENST00000706710.1NIN-2292432No protein-
 
Retained intron
---
ENST00000463419.1NIN-2071317No protein-
 
Retained intron
--TSL:4
ENST00000480476.1NIN-210920No protein-
 
Retained intron
--TSL:3
ENST00000555984.1NIN-216717No protein-
 
Retained intron
--TSL:2
ENST00000474937.1NIN-208533No protein-
 
Retained intron
--TSL:3
Statistics

Exons: 31, Coding exons: 29, Transcript length: 10,334 bps, Translation length: 2,133 residues

MANE

This MANE Select transcript contains ENSP00000436092 and matches to NM_020921.4 and NP_065972.4

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q8N4C6

CCDS

This transcript is a member of the Human CCDS set: CCDS91876

Transcript Support Level (TSL)

TSL:5

Version

ENST00000530997.7

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.