Canonical Allele Identifier: CA435411623

Gene: ARHGAP31

Linked Data

• MyVariant Identifiers: chr3:g.119132969C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414122C>T , CM000665.2:g.119414122C>T	GRCh38
NC_000003.11:g.119132969C>T , CM000665.1:g.119132969C>T	GRCh37
NC_000003.10:g.120615659C>T	NCBI36
NG_007665.2:g.124750C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2193C>T MANE Select	ENSP00000264245.4:p.Ser731=
ENST00000264245.8:c.2193C>T	ENSP00000264245.4:p.Ser731=
NM_020754.3:c.2193C>T	NP_065805.2:p.Ser731=
XM_005247671.3:c.2100C>T	XP_005247728.1:p.Ser700=
XM_006713714.2:c.2133C>T	XP_006713777.1:p.Ser711=
XM_006713714.3:c.2133C>T	XP_006713777.1:p.Ser711=
XM_017006955.1:c.1701C>T	XP_016862444.1:p.Ser567=
NM_020754.4:c.2193C>T MANE Select	NP_065805.2:p.Ser731=