Human (GRCh38.p14)
Description

family with sequence similarity 216 member A [Source:HGNC Symbol;Acc:HGNC:30180]

Gene Synonyms

C12ORF24, HSU79274

Location

Chromosome 12: 110,468,415-110,490,385 forward strand.

GRCh38:CM000674.2

About this gene

This gene has 6 transcripts (splice variants), 93 orthologues and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000377673.10FAM216A-2011101273aaENSP00000366901.5
 
Protein coding
CCDS31899Q8WUB2 NM_013300.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000548449.1FAM216A-20592977aaENSP00000448777.1
 
Nonsense mediated decay
F8VXY8 -TSL:1
ENST00000538285.6FAM216A-2021679No protein-
 
Retained intron
--TSL:1
ENST00000547539.1FAM216A-2041384No protein-
 
Retained intron
--TSL:2
ENST00000548869.1FAM216A-2061160No protein-
 
Retained intron
--TSL:2
ENST00000546396.1FAM216A-203792No protein-
 
Retained intron
--TSL:5