Canonical Allele Identifier: CA1396548628

Gene: ARHGAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414272C= , CM000665.2:g.119414272C=	GRCh38
NC_000003.11:g.119133119C= , CM000665.1:g.119133119C=	GRCh37
NC_000003.10:g.120615809C=	NCBI36
NG_007665.2:g.124900C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2343C= MANE Select	ENSP00000264245.4:p.Leu781=
ENST00000264245.8:c.2343C=	ENSP00000264245.4:p.Leu781=
NM_020754.3:c.2343C=	NP_065805.2:p.Leu781=
XM_005247671.3:c.2250C=	XP_005247728.1:p.Leu750=
XM_006713714.2:c.2283C=	XP_006713777.1:p.Leu761=
XM_006713714.3:c.2283C=	XP_006713777.1:p.Leu761=
XM_017006955.1:c.1851C=	XP_016862444.1:p.Leu617=
NM_020754.4:c.2343C= MANE Select	NP_065805.2:p.Leu781=