Human (GRCh38.p14)
Description

family with sequence similarity 177 member B [Source:HGNC Symbol;Acc:HGNC:34395]

Gene Synonyms

FLJ43505, RP11-452F19.2

About this transcript

This transcript has 6 exons, is associated with 5862 variant alleles and maps to 305 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000445590.4FAM177B-2041677158aaENSP00000414451.2
 
Protein coding
CCDS1535A6PVY3-1 NM_001394345.1MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000360827.6FAM177B-201764158aaENSP00000354070.2
 
Protein coding
CCDS1535A6PVY3-1 -GENCODE basicAPPRIS P1TSL:5
ENST00000456298.5FAM177B-20554599aaENSP00000400233.1
 
Protein coding
A6PVY1 -TSL:4CDS 3' incomplete
ENST00000434700.5FAM177B-203466100aaENSP00000391615.1
 
Protein coding
A6PVY2 -TSL:5CDS 3' incomplete
ENST00000391880.6FAM177B-2021994120aaENSP00000375752.2
 
Nonsense mediated decay
A6PVY3-2 -TSL:2
ENST00000460763.5FAM177B-206582No protein-
 
Retained intron
--TSL:4
Statistics

Exons: 6, Coding exons: 3, Transcript length: 1,994 bps, Translation length: 120 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: A6PVY3

Transcript Support Level (TSL)

TSL:2

Version

ENST00000391880.6

Type

Nonsense mediated decay

Annotation Method

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