Canonical Allele Identifier: CA1396548462

Gene: ARHGAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413872C= , CM000665.2:g.119413872C=	GRCh38
NC_000003.11:g.119132719C= , CM000665.1:g.119132719C=	GRCh37
NC_000003.10:g.120615409C=	NCBI36
NG_007665.2:g.124500C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1943C= MANE Select	ENSP00000264245.4:p.Ala648=
ENST00000264245.8:c.1943C=	ENSP00000264245.4:p.Ala648=
NM_020754.3:c.1943C=	NP_065805.2:p.Ala648=
XM_005247671.3:c.1850C=	XP_005247728.1:p.Ala617=
XM_006713714.2:c.1883C=	XP_006713777.1:p.Ala628=
XM_006713714.3:c.1883C=	XP_006713777.1:p.Ala628=
XM_017006955.1:c.1451C=	XP_016862444.1:p.Ala484=
NM_020754.4:c.1943C= MANE Select	NP_065805.2:p.Ala648=