Canonical Allele Identifier: CA2573136474

Gene: ARHGAP31

Linked Data

• ClinVar Variation Id: 1548158
• ClinVar RCV Id: RCV002165863
• dbSNP Id: rs2107631521

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119382279C>A , CM000665.2:g.119382279C>A	GRCh38
NC_000003.11:g.119101126C>A , CM000665.1:g.119101126C>A	GRCh37
NC_000003.10:g.120583816C>A	NCBI36
NG_007665.2:g.92907C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.432-13C>A MANE Select	ENSP00000264245.4:n.432-13C>A
ENST00000264245.8:c.432-13C>A	ENSP00000264245.4:n.432-13C>A
ENST00000482743.1:c.345-13C>A	ENSP00000418429.1:n.345-13C>A
NM_020754.3:c.432-13C>A	NP_065805.2:n.432-13C>A
XM_005247671.3:c.339-13C>A	XP_005247728.1:n.339-13C>A
XM_006713714.2:c.432-13C>A	XP_006713777.1:n.432-13C>A
XM_006713714.3:c.432-13C>A	XP_006713777.1:n.432-13C>A
XM_017006955.1:c.-61-13C>A	XP_016862444.1:n.-61-13C>A
NM_020754.4:c.432-13C>A MANE Select	NP_065805.2:n.432-13C>A