Canonical Allele Identifier: CA1396548697

Gene: ARHGAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414429T= , CM000665.2:g.119414429T=	GRCh38
NC_000003.11:g.119133276T= , CM000665.1:g.119133276T=	GRCh37
NC_000003.10:g.120615966T=	NCBI36
NG_007665.2:g.125057T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2500T= MANE Select	ENSP00000264245.4:p.Cys834=
ENST00000264245.8:c.2500T=	ENSP00000264245.4:p.Cys834=
NM_020754.3:c.2500T=	NP_065805.2:p.Cys834=
XM_005247671.3:c.2407T=	XP_005247728.1:p.Cys803=
XM_006713714.2:c.2440T=	XP_006713777.1:p.Cys814=
XM_006713714.3:c.2440T=	XP_006713777.1:p.Cys814=
XM_017006955.1:c.2008T=	XP_016862444.1:p.Cys670=
NM_020754.4:c.2500T= MANE Select	NP_065805.2:p.Cys834=