Canonical Allele Identifier: CA435411830

Gene: ARHGAP31

Linked Data

• MyVariant Identifiers: chr3:g.119133128T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414281T>A , CM000665.2:g.119414281T>A	GRCh38
NC_000003.11:g.119133128T>A , CM000665.1:g.119133128T>A	GRCh37
NC_000003.10:g.120615818T>A	NCBI36
NG_007665.2:g.124909T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2352T>A MANE Select	ENSP00000264245.4:p.Ala784=
ENST00000264245.8:c.2352T>A	ENSP00000264245.4:p.Ala784=
NM_020754.3:c.2352T>A	NP_065805.2:p.Ala784=
XM_005247671.3:c.2259T>A	XP_005247728.1:p.Ala753=
XM_006713714.2:c.2292T>A	XP_006713777.1:p.Ala764=
XM_006713714.3:c.2292T>A	XP_006713777.1:p.Ala764=
XM_017006955.1:c.1860T>A	XP_016862444.1:p.Ala620=
NM_020754.4:c.2352T>A MANE Select	NP_065805.2:p.Ala784=