Canonical Allele Identifier: CA1396548692

Gene: ARHGAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414416G= , CM000665.2:g.119414416G=	GRCh38
NC_000003.11:g.119133263G= , CM000665.1:g.119133263G=	GRCh37
NC_000003.10:g.120615953G=	NCBI36
NG_007665.2:g.125044G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2487G= MANE Select	ENSP00000264245.4:p.Glu829=
ENST00000264245.8:c.2487G=	ENSP00000264245.4:p.Glu829=
NM_020754.3:c.2487G=	NP_065805.2:p.Glu829=
XM_005247671.3:c.2394G=	XP_005247728.1:p.Glu798=
XM_006713714.2:c.2427G=	XP_006713777.1:p.Glu809=
XM_006713714.3:c.2427G=	XP_006713777.1:p.Glu809=
XM_017006955.1:c.1995G=	XP_016862444.1:p.Glu665=
NM_020754.4:c.2487G= MANE Select	NP_065805.2:p.Glu829=