Canonical Allele Identifier: CA1396548951

Gene: ARHGAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119415097G= , CM000665.2:g.119415097G=	GRCh38
NC_000003.11:g.119133944G= , CM000665.1:g.119133944G=	GRCh37
NC_000003.10:g.120616634G=	NCBI36
NG_007665.2:g.125725G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.3168G= MANE Select	ENSP00000264245.4:p.Gln1056=
ENST00000264245.8:c.3168G=	ENSP00000264245.4:p.Gln1056=
NM_020754.3:c.3168G=	NP_065805.2:p.Gln1056=
XM_005247671.3:c.3075G=	XP_005247728.1:p.Gln1025=
XM_006713714.2:c.3108G=	XP_006713777.1:p.Gln1036=
XM_006713714.3:c.3108G=	XP_006713777.1:p.Gln1036=
XM_017006955.1:c.2676G=	XP_016862444.1:p.Gln892=
NM_020754.4:c.3168G= MANE Select	NP_065805.2:p.Gln1056=