Canonical Allele Identifier: CA1396548624

Gene: ARHGAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414264C= , CM000665.2:g.119414264C=	GRCh38
NC_000003.11:g.119133111C= , CM000665.1:g.119133111C=	GRCh37
NC_000003.10:g.120615801C=	NCBI36
NG_007665.2:g.124892C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2335C= MANE Select	ENSP00000264245.4:p.Pro779=
ENST00000264245.8:c.2335C=	ENSP00000264245.4:p.Pro779=
NM_020754.3:c.2335C=	NP_065805.2:p.Pro779=
XM_005247671.3:c.2242C=	XP_005247728.1:p.Pro748=
XM_006713714.2:c.2275C=	XP_006713777.1:p.Pro759=
XM_006713714.3:c.2275C=	XP_006713777.1:p.Pro759=
XM_017006955.1:c.1843C=	XP_016862444.1:p.Pro615=
NM_020754.4:c.2335C= MANE Select	NP_065805.2:p.Pro779=