Canonical Allele Identifier: CA435411669

Gene: ARHGAP31

Linked Data

• MyVariant Identifiers: chr3:g.119133032G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414185G>T , CM000665.2:g.119414185G>T	GRCh38
NC_000003.11:g.119133032G>T , CM000665.1:g.119133032G>T	GRCh37
NC_000003.10:g.120615722G>T	NCBI36
NG_007665.2:g.124813G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2256G>T MANE Select	ENSP00000264245.4:p.Leu752=
ENST00000264245.8:c.2256G>T	ENSP00000264245.4:p.Leu752=
NM_020754.3:c.2256G>T	NP_065805.2:p.Leu752=
XM_005247671.3:c.2163G>T	XP_005247728.1:p.Leu721=
XM_006713714.2:c.2196G>T	XP_006713777.1:p.Leu732=
XM_006713714.3:c.2196G>T	XP_006713777.1:p.Leu732=
XM_017006955.1:c.1764G>T	XP_016862444.1:p.Leu588=
NM_020754.4:c.2256G>T MANE Select	NP_065805.2:p.Leu752=