Canonical Allele Identifier: CA435411907

Gene: ARHGAP31

Linked Data

• ClinVar Variation Id: 1642709
• ClinVar RCV Id: RCV002145682
• dbSNP Id: rs113966268
• gnomAD v4: 3-119414416-G-A
• MyVariant Identifiers: chr3:g.119133263G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414416G>A , CM000665.2:g.119414416G>A	GRCh38
NC_000003.11:g.119133263G>A , CM000665.1:g.119133263G>A	GRCh37
NC_000003.10:g.120615953G>A	NCBI36
NG_007665.2:g.125044G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2487G>A MANE Select	ENSP00000264245.4:p.Glu829=
ENST00000264245.8:c.2487G>A	ENSP00000264245.4:p.Glu829=
NM_020754.3:c.2487G>A	NP_065805.2:p.Glu829=
XM_005247671.3:c.2394G>A	XP_005247728.1:p.Glu798=
XM_006713714.2:c.2427G>A	XP_006713777.1:p.Glu809=
XM_006713714.3:c.2427G>A	XP_006713777.1:p.Glu809=
XM_017006955.1:c.1995G>A	XP_016862444.1:p.Glu665=
NM_020754.4:c.2487G>A MANE Select	NP_065805.2:p.Glu829=