Human (GRCh38.p14)
Description

tumor suppressing subtransferable candidate 4 [Source:HGNC Symbol;Acc:HGNC:12386]

Location
About this transcript

This transcript has 3 exons, is annotated with 12 domains and features, is associated with 2064 variant alleles and maps to 381 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000333256.11TSSC4-2011472329aaENSP00000331087.6
 
Protein coding
CCDS7735Q9Y5U2-1 NM_005706.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P2TSL:1
ENST00000380996.9TSSC4-2031544265aaENSP00000370384.5
 
Protein coding
CCDS73241Q9Y5U2-2 -GENCODE basicAPPRIS ALT2TSL:1
ENST00000451491.2TSSC4-2071423329aaENSP00000411224.2
 
Protein coding
CCDS7735Q9Y5U2-1 -GENCODE basicAPPRIS P2TSL:1
ENST00000380992.5TSSC4-202992127aaENSP00000370380.1
 
Protein coding
A6NCC9 -GENCODE basicTSL:5
ENST00000485682.6TSSC4-209979110aaENSP00000431430.1
 
Protein coding
E9PL88 -TSL:2CDS 3' incomplete
ENST00000437110.5TSSC4-205974203aaENSP00000396925.1
 
Protein coding
C9JHT9 -TSL:2CDS 3' incomplete
ENST00000496468.1TSSC4-210912191aaENSP00000435013.1
 
Protein coding
E9PME3 -TSL:1CDS 3' incomplete
ENST00000435795.5TSSC4-204863112aaENSP00000403475.1
 
Protein coding
C9JDU0 -TSL:3CDS 3' incomplete
ENST00000440813.1TSSC4-206851207aaENSP00000416937.1
 
Protein coding
C9JJV1 -TSL:3CDS 3' incomplete
ENST00000467308.1TSSC4-208409No protein-
 
Protein coding CDS not defined
--TSL:3
Statistics

Exons: 3, Coding exons: 1, Transcript length: 1,472 bps, Translation length: 329 residues

MANE

This MANE Select transcript contains ENSP00000331087 and matches to NM_005706.4 and NP_005697.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9Y5U2

CCDS

This transcript is a member of the Human CCDS set: CCDS7735

Transcript Support Level (TSL)

TSL:1

Version

ENST00000333256.11

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.