Canonical Allele Identifier: CA2667110213

Gene: ARHGAP31

Linked Data

• gnomAD v4: 3-119413731-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413731_119413732insC , CM000665.2:g.119413731_119413732insC	GRCh38
NC_000003.11:g.119132578_119132579insC , CM000665.1:g.119132578_119132579insC	GRCh37
NC_000003.10:g.120615268_120615269insC	NCBI36
NG_007665.2:g.124359_124360insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1927-125_1927-124insC MANE Select	ENSP00000264245.4:n.1927-125_1927-124insC
ENST00000264245.8:c.1927-125_1927-124insC	ENSP00000264245.4:n.1927-125_1927-124insC
NM_020754.3:c.1927-125_1927-124insC	NP_065805.2:n.1927-125_1927-124insC
XM_005247671.3:c.1834-125_1834-124insC	XP_005247728.1:n.1834-125_1834-124insC
XM_006713714.2:c.1867-125_1867-124insC	XP_006713777.1:n.1867-125_1867-124insC
XM_006713714.3:c.1867-125_1867-124insC	XP_006713777.1:n.1867-125_1867-124insC
XM_017006955.1:c.1435-125_1435-124insC	XP_016862444.1:n.1435-125_1435-124insC
NM_020754.4:c.1927-125_1927-124insC MANE Select	NP_065805.2:n.1927-125_1927-124insC