Human (GRCh38.p14)
Description

family with sequence similarity 227 member A [Source:HGNC Symbol;Acc:HGNC:44197]

Location

Chromosome 22: 38,578,118-38,656,629 reverse strand.

GRCh38:CM000684.2

About this gene

This gene has 11 transcripts (splice variants) and 88 orthologues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000535113.7FAM227A-20510087570aaENSP00000445093.1
 
Protein coding
CCDS93164F5H4B4-1 NM_001013647.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS ALT2TSL:5
ENST00000540952.6FAM227A-20610396622aaENSP00000493504.1
 
Protein coding
A0A2R8YCE3 -GENCODE basicAPPRIS ALT2TSL:5
ENST00000355830.11FAM227A-2012414651aaENSP00000348086.7
 
Protein coding
A0A0A0MRD0 -GENCODE basicAPPRIS P4TSL:5
ENST00000544346.5FAM227A-2101957No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000541689.6FAM227A-2071259No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000424706.5FAM227A-202596No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000543295.1FAM227A-208582No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000608409.5FAM227A-211562No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000543828.1FAM227A-209497No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000484582.1FAM227A-203642No protein-
 
Retained intron
--TSL:3
ENST00000490082.1FAM227A-204561No protein-
 
Retained intron
--TSL:4