Canonical Allele Identifier: CA1396548642

Gene: ARHGAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414301T= , CM000665.2:g.119414301T=	GRCh38
NC_000003.11:g.119133148T= , CM000665.1:g.119133148T=	GRCh37
NC_000003.10:g.120615838T=	NCBI36
NG_007665.2:g.124929T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2372T= MANE Select	ENSP00000264245.4:p.Leu791=
ENST00000264245.8:c.2372T=	ENSP00000264245.4:p.Leu791=
NM_020754.3:c.2372T=	NP_065805.2:p.Leu791=
XM_005247671.3:c.2279T=	XP_005247728.1:p.Leu760=
XM_006713714.2:c.2312T=	XP_006713777.1:p.Leu771=
XM_006713714.3:c.2312T=	XP_006713777.1:p.Leu771=
XM_017006955.1:c.1880T=	XP_016862444.1:p.Leu627=
NM_020754.4:c.2372T= MANE Select	NP_065805.2:p.Leu791=