Advanced notice of Ensembl Tools maintenance
Please note that due to planned maintenance, Ensembl Tools will be unavailable from Tuesday, September 9, at 08:30 AM BST until Wednesday, September 10, at 08:30 AM BST.
Jobs submitted during the maintenance window will be queued and processed once maintenance is complete. We apologise for the inconvenience.

Human (GRCh38.p14)
Description

family with sequence similarity 171 member A2 [Source:HGNC Symbol;Acc:HGNC:30480]

Gene Synonyms

MGC34829

Location

Chromosome 17: 44,353,215-44,363,853 reverse strand.

GRCh38:CM000679.2

About this gene

This gene has 4 transcripts (splice variants), 206 orthologues and 2 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000293443.12FAM171A2-2013138826aaENSP00000293443.6
 
Protein coding
CCDS45701A8MVW0 NM_198475.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000589407.5FAM171A2-2031066159aaENSP00000466195.1
 
Nonsense mediated decay
K7EMG4 -TSL:3
ENST00000588067.1FAM171A2-202964159aaENSP00000466493.1
 
Nonsense mediated decay
K7EMG4 -TSL:5
ENST00000592560.1FAM171A2-204758No protein-
 
Retained intron
--TSL:2