Human (GRCh38.p14)
Description

family with sequence similarity 149 member B1 [Source:HGNC Symbol;Acc:HGNC:29162]

Gene Synonyms

KIAA0974

Location
About this transcript

This transcript has 3 exons, is associated with 3085 variant alleles and maps to 137 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000242505.11FAM149B1-2015455582aaENSP00000242505.6
 
Protein coding
CCDS44435Q96BN6-1 NM_173348.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000445951.5FAM149B1-2032169335aaENSP00000402293.1
 
Protein coding
H0Y607 -TSL:5CDS 5' incomplete
ENST00000372955.7FAM149B1-2021534469aaENSP00000362046.3
 
Protein coding
H7BY93 -TSL:1CDS 5' incomplete
ENST00000475829.5FAM149B1-2071044209aaENSP00000476913.1
 
Nonsense mediated decay
V9GYM5 -TSL:5CDS 5' incomplete
ENST00000607940.1FAM149B1-208834No protein-
 
Protein coding CDS not defined
--TSL:NA
ENST00000470798.5FAM149B1-206491No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000468462.1FAM149B1-2052520No protein-
 
Retained intron
--TSL:2
ENST00000466261.1FAM149B1-204696No protein-
 
Retained intron
--TSL:3
Statistics

Exons: 3, Coding exons: 0, Transcript length: 491 bps,

Transcript Support Level (TSL)

TSL:3

Version

ENST00000470798.5

Type

Protein coding CDS not defined

Annotation Method

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