Canonical Allele Identifier: CA435411868

Gene: ARHGAP31

Linked Data

• MyVariant Identifiers: chr3:g.119133143T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414296T>G , CM000665.2:g.119414296T>G	GRCh38
NC_000003.11:g.119133143T>G , CM000665.1:g.119133143T>G	GRCh37
NC_000003.10:g.120615833T>G	NCBI36
NG_007665.2:g.124924T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2367T>G MANE Select	ENSP00000264245.4:p.Thr789=
ENST00000264245.8:c.2367T>G	ENSP00000264245.4:p.Thr789=
NM_020754.3:c.2367T>G	NP_065805.2:p.Thr789=
XM_005247671.3:c.2274T>G	XP_005247728.1:p.Thr758=
XM_006713714.2:c.2307T>G	XP_006713777.1:p.Thr769=
XM_006713714.3:c.2307T>G	XP_006713777.1:p.Thr769=
XM_017006955.1:c.1875T>G	XP_016862444.1:p.Thr625=
NM_020754.4:c.2367T>G MANE Select	NP_065805.2:p.Thr789=