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 5 exons, is associated with 11024 variant alleles and maps to 115 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: 5, Coding exons: 0, Transcript length: 541 bps,

Transcript Support Level (TSL)

TSL:3

Version

ENST00000507084.1

Type

Protein coding CDS not defined

Annotation Method

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