Canonical Allele Identifier: CA1396548990

Gene: ARHGAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119415196G= , CM000665.2:g.119415196G=	GRCh38
NC_000003.11:g.119134043G= , CM000665.1:g.119134043G=	GRCh37
NC_000003.10:g.120616733G=	NCBI36
NG_007665.2:g.125824G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.3267G= MANE Select	ENSP00000264245.4:p.Gln1089=
ENST00000264245.8:c.3267G=	ENSP00000264245.4:p.Gln1089=
NM_020754.3:c.3267G=	NP_065805.2:p.Gln1089=
XM_005247671.3:c.3174G=	XP_005247728.1:p.Gln1058=
XM_006713714.2:c.3207G=	XP_006713777.1:p.Gln1069=
XM_006713714.3:c.3207G=	XP_006713777.1:p.Gln1069=
XM_017006955.1:c.2775G=	XP_016862444.1:p.Gln925=
NM_020754.4:c.3267G= MANE Select	NP_065805.2:p.Gln1089=