Canonical Allele Identifier: CA2667110177

Gene: ARHGAP31

Linked Data

• gnomAD v4: 3-119413707-AAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413709_119413710del , CM000665.2:g.119413709_119413710del	GRCh38
NC_000003.11:g.119132556_119132557del , CM000665.1:g.119132556_119132557del	GRCh37
NC_000003.10:g.120615246_120615247del	NCBI36
NG_007665.2:g.124337_124338del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1927-147_1927-146del MANE Select	ENSP00000264245.4:n.1927-147_1927-146del
ENST00000264245.8:c.1927-147_1927-146del	ENSP00000264245.4:n.1927-147_1927-146del
NM_020754.3:c.1927-147_1927-146del	NP_065805.2:n.1927-147_1927-146del
XM_005247671.3:c.1834-147_1834-146del	XP_005247728.1:n.1834-147_1834-146del
XM_006713714.2:c.1867-147_1867-146del	XP_006713777.1:n.1867-147_1867-146del
XM_006713714.3:c.1867-147_1867-146del	XP_006713777.1:n.1867-147_1867-146del
XM_017006955.1:c.1435-147_1435-146del	XP_016862444.1:n.1435-147_1435-146del
NM_020754.4:c.1927-147_1927-146del MANE Select	NP_065805.2:n.1927-147_1927-146del