Human (GRCh38.p14)
Description

family with sequence similarity 151 member B [Source:HGNC Symbol;Acc:HGNC:33716]

Gene Synonyms

UNQ9217

Location
About this transcript

This transcript has 6 exons, is annotated with 3 domains and features, is associated with 23676 variant alleles and maps to 225 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000282226.5FAM151B-2011586276aaENSP00000282226.4
 
Protein coding
CCDS4051Q6UXP7 NM_205548.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000502608.5FAM151B-20250867aaENSP00000427035.1
 
Nonsense mediated decay
D6RD51 -TSL:3
ENST00000511718.5FAM151B-2052185No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000507084.1FAM151B-203541No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000509292.1FAM151B-2041019No protein-
 
Retained intron
--TSL:3
Statistics

Exons: 6, Coding exons: 6, Transcript length: 1,586 bps, Translation length: 276 residues

MANE

This MANE Select transcript contains ENSP00000282226 and matches to NM_205548.3 and NP_991111.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q6UXP7

CCDS

This transcript is a member of the Human CCDS set: CCDS4051

Transcript Support Level (TSL)

TSL:1

Version

ENST00000282226.5

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

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