Human (GRCh38.p14)
Description

family with sequence similarity 78 member B [Source:HGNC Symbol;Acc:HGNC:13495]

About this transcript

This transcript has 3 exons, is associated with 48131 variant alleles and maps to 248 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000354422.4FAM78B-2022481261aaENSP00000346404.3
 
Protein coding
CCDS30931Q5VT40 NM_001017961.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:2
ENST00000338353.4FAM78B-2011596261aaENSP00000339681.3
 
Protein coding
CCDS30931Q5VT40 -GENCODE basicAPPRIS P1TSL:1
ENST00000435676.2FAM78B-2034410254aaENSP00000412766.1
 
Nonsense mediated decay
H7C3M6 -TSL:2CDS 5' incomplete
ENST00000456900.1FAM78B-2052300261aaENSP00000389945.1
 
Nonsense mediated decay
CCDS30931Q5VT40 -TSL:5
ENST00000441649.1FAM78B-2042264257aaENSP00000393329.1
 
Nonsense mediated decay
H7C075 -TSL:5CDS 5' incomplete
Statistics

Exons: 3, Coding exons: 2, Transcript length: 2,300 bps, Translation length: 261 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q5VT40

CCDS

This transcript is a member of the Human CCDS set: CCDS30931

Transcript Support Level (TSL)

TSL:5

Version

ENST00000456900.1

Type

Nonsense mediated decay

Annotation Method

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