Human (GRCh37.p13)
Description

family with sequence similarity 166, member A [Source:HGNC Symbol;Acc:33818]

Location

Chromosome 9: 140,138,036-140,142,222 reverse strand.

GRCh37:CM000671.1

About this gene

This gene has 4 transcripts (splice variants) and 116 orthologues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000344774.4FAM166A-0011124317aaENSP00000344729.4
 
Protein coding
CCDS35186Q6J272 NM_001001710.1Ensembl CanonicalGENCODE Basic
ENST00000388932.2FAM166A-201871271aaENSP00000373584.2
 
Protein coding
Q6J272 -GENCODE Basic
ENST00000484720.1FAM166A-003705223aaENSP00000420741.1
 
Protein coding
C9JBW9 -CDS 3' incomplete
ENST00000471784.1FAM166A-0021720271aaENSP00000419151.1
 
Nonsense mediated decay
Q6J272 --