Canonical Allele Identifier: CA1396548685

Gene: ARHGAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414404A= , CM000665.2:g.119414404A=	GRCh38
NC_000003.11:g.119133251A= , CM000665.1:g.119133251A=	GRCh37
NC_000003.10:g.120615941A=	NCBI36
NG_007665.2:g.125032A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2475A= MANE Select	ENSP00000264245.4:p.Gln825=
ENST00000264245.8:c.2475A=	ENSP00000264245.4:p.Gln825=
NM_020754.3:c.2475A=	NP_065805.2:p.Gln825=
XM_005247671.3:c.2382A=	XP_005247728.1:p.Gln794=
XM_006713714.2:c.2415A=	XP_006713777.1:p.Gln805=
XM_006713714.3:c.2415A=	XP_006713777.1:p.Gln805=
XM_017006955.1:c.1983A=	XP_016862444.1:p.Gln661=
NM_020754.4:c.2475A= MANE Select	NP_065805.2:p.Gln825=