Human (GRCh38.p14)
Description

family with sequence similarity 86 member B2 [Source:HGNC Symbol;Acc:HGNC:32222]

Location
About this transcript

This transcript has 8 exons, is annotated with 6 domains and features, is associated with 7927 variant alleles and maps to 1384 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000262365.9FAM86B2-2012518330aaENSP00000262365.4
 
Protein coding
CCDS59092P0C5J1 NM_001137610.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000685726.1FAM86B2-205222371aaENSP00000508501.1
 
Nonsense mediated decay
A0A8I5KNE8 -CDS 5' incomplete
ENST00000687060.1FAM86B2-2062158153aaENSP00000510323.1
 
Nonsense mediated decay
---
ENST00000687949.1FAM86B2-2072017126aaENSP00000510499.1
 
Nonsense mediated decay
A0A8I5KZ44 --
ENST00000527331.6FAM86B2-2031295187aaENSP00000432491.2
 
Nonsense mediated decay
E9PQV7 -TSL:5
ENST00000532480.6FAM86B2-2041171105aaENSP00000436338.2
 
Nonsense mediated decay
E9PM45 -TSL:2
ENST00000309608.7FAM86B2-20295366aaENSP00000311330.7
 
Nonsense mediated decay
E9PLW5 -TSL:3
Statistics

Exons: 8, Coding exons: 8, Transcript length: 2,518 bps, Translation length: 330 residues

MANE

This MANE Select transcript contains ENSP00000262365 and matches to NM_001137610.3 and NP_001131082.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: P0C5J1

CCDS

This transcript is a member of the Human CCDS set: CCDS59092

Transcript Support Level (TSL)

TSL:5

Version

ENST00000262365.9

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.

Annotation Attributes

RNA-Seq supported only [Definitions]

GENCODE basic gene

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