Canonical Allele Identifier: CA1396548586

Gene: ARHGAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414176C= , CM000665.2:g.119414176C=	GRCh38
NC_000003.11:g.119133023C= , CM000665.1:g.119133023C=	GRCh37
NC_000003.10:g.120615713C=	NCBI36
NG_007665.2:g.124804C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2247C= MANE Select	ENSP00000264245.4:p.Leu749=
ENST00000264245.8:c.2247C=	ENSP00000264245.4:p.Leu749=
NM_020754.3:c.2247C=	NP_065805.2:p.Leu749=
XM_005247671.3:c.2154C=	XP_005247728.1:p.Leu718=
XM_006713714.2:c.2187C=	XP_006713777.1:p.Leu729=
XM_006713714.3:c.2187C=	XP_006713777.1:p.Leu729=
XM_017006955.1:c.1755C=	XP_016862444.1:p.Leu585=
NM_020754.4:c.2247C= MANE Select	NP_065805.2:p.Leu749=