Human (GRCh37.p13)
Description

family with sequence similarity 166, member B [Source:HGNC Symbol;Acc:34242]

Location
About this transcript

This transcript has 6 exons, is annotated with 6 domains and features, is associated with 865 variant alleles and maps to 226 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000399742.2FAM166B-005958275aaENSP00000382646.2
 
Protein coding
CCDS56572A8MTA8 NM_001164310.1GENCODE basic
ENST00000447837.1FAM166B-004889216aaENSP00000412746.1
 
Nonsense mediated decay
CCDS47963A8MTA8 --
ENST00000492890.1FAM166B-001971No protein-
 
Processed transcript
---
ENST00000480287.1FAM166B-002681No protein-
 
Processed transcript
---
ENST00000478246.1FAM166B-003627No protein-
 
Processed transcript
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Statistics

Exons: 6, Coding exons: 6, Transcript length: 958 bps, Translation length: 275 residues

CCDS

This transcript is a member of the Human CCDS set: CCDS56572

Uniprot

This transcript corresponds to the following Uniprot identifiers: A8MTA8

Version

ENST00000399742.2

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.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Transcript having exact match between ENSEMBL and HAVANA:
OTTHUMT00000336563 (version 1)
GENCODE basic gene

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