Canonical Allele Identifier: CA435411855

Gene: ARHGAP31

Linked Data

• MyVariant Identifiers: chr3:g.119133137T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414290T>G , CM000665.2:g.119414290T>G	GRCh38
NC_000003.11:g.119133137T>G , CM000665.1:g.119133137T>G	GRCh37
NC_000003.10:g.120615827T>G	NCBI36
NG_007665.2:g.124918T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2361T>G MANE Select	ENSP00000264245.4:p.Pro787=
ENST00000264245.8:c.2361T>G	ENSP00000264245.4:p.Pro787=
NM_020754.3:c.2361T>G	NP_065805.2:p.Pro787=
XM_005247671.3:c.2268T>G	XP_005247728.1:p.Pro756=
XM_006713714.2:c.2301T>G	XP_006713777.1:p.Pro767=
XM_006713714.3:c.2301T>G	XP_006713777.1:p.Pro767=
XM_017006955.1:c.1869T>G	XP_016862444.1:p.Pro623=
NM_020754.4:c.2361T>G MANE Select	NP_065805.2:p.Pro787=