Canonical Allele Identifier: CA1396548598

Gene: ARHGAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414202T= , CM000665.2:g.119414202T=	GRCh38
NC_000003.11:g.119133049T= , CM000665.1:g.119133049T=	GRCh37
NC_000003.10:g.120615739T=	NCBI36
NG_007665.2:g.124830T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2273T= MANE Select	ENSP00000264245.4:p.Val758=
ENST00000264245.8:c.2273T=	ENSP00000264245.4:p.Val758=
NM_020754.3:c.2273T=	NP_065805.2:p.Val758=
XM_005247671.3:c.2180T=	XP_005247728.1:p.Val727=
XM_006713714.2:c.2213T=	XP_006713777.1:p.Val738=
XM_006713714.3:c.2213T=	XP_006713777.1:p.Val738=
XM_017006955.1:c.1781T=	XP_016862444.1:p.Val594=
NM_020754.4:c.2273T= MANE Select	NP_065805.2:p.Val758=