Canonical Allele Identifier: CA1396548560

Gene: ARHGAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414128A= , CM000665.2:g.119414128A=	GRCh38
NC_000003.11:g.119132975A= , CM000665.1:g.119132975A=	GRCh37
NC_000003.10:g.120615665A=	NCBI36
NG_007665.2:g.124756A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2199A= MANE Select	ENSP00000264245.4:p.Ala733=
ENST00000264245.8:c.2199A=	ENSP00000264245.4:p.Ala733=
NM_020754.3:c.2199A=	NP_065805.2:p.Ala733=
XM_005247671.3:c.2106A=	XP_005247728.1:p.Ala702=
XM_006713714.2:c.2139A=	XP_006713777.1:p.Ala713=
XM_006713714.3:c.2139A=	XP_006713777.1:p.Ala713=
XM_017006955.1:c.1707A=	XP_016862444.1:p.Ala569=
NM_020754.4:c.2199A= MANE Select	NP_065805.2:p.Ala733=