Canonical Allele Identifier: CA354039888

Gene: ARHGAP31

Linked Data

• MyVariant Identifiers: chr3:g.119121128G>T (hg19) ; chr3:g.119402281G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119402281G>T , CM000665.2:g.119402281G>T	GRCh38
NC_000003.11:g.119121128G>T , CM000665.1:g.119121128G>T	GRCh37
NC_000003.10:g.120603818G>T	NCBI36
NG_007665.2:g.112909G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264245.9:c.1529G>T MANE Select	ENSP00000264245.4:p.Arg510Ile
ENST00000264245.8:c.1529G>T	ENSP00000264245.4:p.Arg510Ile
NM_020754.3:c.1529G>T	NP_065805.2:p.Arg510Ile
XM_005247671.3:c.1436G>T	XP_005247728.1:p.Arg479Ile
XM_006713714.2:c.1469G>T	XP_006713777.1:p.Arg490Ile
XM_006713714.3:c.1469G>T	XP_006713777.1:p.Arg490Ile
XM_017006955.1:c.1037G>T	XP_016862444.1:p.Arg346Ile
NM_020754.4:c.1529G>T MANE Select	NP_065805.2:p.Arg510Ile