Canonical Allele Identifier: CA1396548652

Gene: ARHGAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414322T= , CM000665.2:g.119414322T=	GRCh38
NC_000003.11:g.119133169T= , CM000665.1:g.119133169T=	GRCh37
NC_000003.10:g.120615859T=	NCBI36
NG_007665.2:g.124950T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2393T= MANE Select	ENSP00000264245.4:p.Leu798=
ENST00000264245.8:c.2393T=	ENSP00000264245.4:p.Leu798=
NM_020754.3:c.2393T=	NP_065805.2:p.Leu798=
XM_005247671.3:c.2300T=	XP_005247728.1:p.Leu767=
XM_006713714.2:c.2333T=	XP_006713777.1:p.Leu778=
XM_006713714.3:c.2333T=	XP_006713777.1:p.Leu778=
XM_017006955.1:c.1901T=	XP_016862444.1:p.Leu634=
NM_020754.4:c.2393T= MANE Select	NP_065805.2:p.Leu798=