Canonical Allele Identifier: CA1396548463

Gene: ARHGAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413874A= , CM000665.2:g.119413874A=	GRCh38
NC_000003.11:g.119132721A= , CM000665.1:g.119132721A=	GRCh37
NC_000003.10:g.120615411A=	NCBI36
NG_007665.2:g.124502A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1945A= MANE Select	ENSP00000264245.4:p.Asn649=
ENST00000264245.8:c.1945A=	ENSP00000264245.4:p.Asn649=
NM_020754.3:c.1945A=	NP_065805.2:p.Asn649=
XM_005247671.3:c.1852A=	XP_005247728.1:p.Asn618=
XM_006713714.2:c.1885A=	XP_006713777.1:p.Asn629=
XM_006713714.3:c.1885A=	XP_006713777.1:p.Asn629=
XM_017006955.1:c.1453A=	XP_016862444.1:p.Asn485=
NM_020754.4:c.1945A= MANE Select	NP_065805.2:p.Asn649=