Canonical Allele Identifier: CA435412138

Gene: ARHGAP31

Linked Data

• gnomAD v4: 3-119414392-G-A
• COSMIC: COSM6300736
• MyVariant Identifiers: chr3:g.119133239G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414392G>A , CM000665.2:g.119414392G>A	GRCh38
NC_000003.11:g.119133239G>A , CM000665.1:g.119133239G>A	GRCh37
NC_000003.10:g.120615929G>A	NCBI36
NG_007665.2:g.125020G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2463G>A MANE Select	ENSP00000264245.4:p.Gln821=
ENST00000264245.8:c.2463G>A	ENSP00000264245.4:p.Gln821=
NM_020754.3:c.2463G>A	NP_065805.2:p.Gln821=
XM_005247671.3:c.2370G>A	XP_005247728.1:p.Gln790=
XM_006713714.2:c.2403G>A	XP_006713777.1:p.Gln801=
XM_006713714.3:c.2403G>A	XP_006713777.1:p.Gln801=
XM_017006955.1:c.1971G>A	XP_016862444.1:p.Gln657=
NM_020754.4:c.2463G>A MANE Select	NP_065805.2:p.Gln821=