Canonical Allele Identifier: CA1396548667

Gene: ARHGAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414355C= , CM000665.2:g.119414355C=	GRCh38
NC_000003.11:g.119133202C= , CM000665.1:g.119133202C=	GRCh37
NC_000003.10:g.120615892C=	NCBI36
NG_007665.2:g.124983C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2426C= MANE Select	ENSP00000264245.4:p.Ser809=
ENST00000264245.8:c.2426C=	ENSP00000264245.4:p.Ser809=
NM_020754.3:c.2426C=	NP_065805.2:p.Ser809=
XM_005247671.3:c.2333C=	XP_005247728.1:p.Ser778=
XM_006713714.2:c.2366C=	XP_006713777.1:p.Ser789=
XM_006713714.3:c.2366C=	XP_006713777.1:p.Ser789=
XM_017006955.1:c.1934C=	XP_016862444.1:p.Ser645=
NM_020754.4:c.2426C= MANE Select	NP_065805.2:p.Ser809=