Human (GRCh38.p14)
Description

family with sequence similarity 221 member B [Source:HGNC Symbol;Acc:HGNC:30762]

Gene Synonyms

C9ORF128

Location
About this transcript

This transcript has 7 exons, is annotated with 11 domains and features, is associated with 5268 variant alleles and maps to 434 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000423537.7FAM221B-2033557402aaENSP00000415299.2
 
Protein coding
CCDS43799A6H8Z2-1 NM_001012446.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000377984.2FAM221B-2011167301aaENSP00000367222.2
 
Protein coding
F8W8N9 -TSL:1CDS 3' incomplete
ENST00000472182.1FAM221B-20471990aaENSP00000420279.1
 
Protein coding
C9JPK8 -TSL:3CDS 3' incomplete
ENST00000388950.8FAM221B-2023763340aaENSP00000373602.4
 
Nonsense mediated decay
A6H8Z2-3 -TSL:1
Statistics

Exons: 7, Coding exons: 6, Transcript length: 3,557 bps, Translation length: 402 residues

MANE

This MANE Select transcript contains ENSP00000415299 and matches to NM_001012446.4 and NP_001012448.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: A6H8Z2

CCDS

This transcript is a member of the Human CCDS set: CCDS43799

Transcript Support Level (TSL)

TSL:1

Version

ENST00000423537.7

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.