Canonical Allele Identifier: CA2667110200

Gene: ARHGAP31

Linked Data

• gnomAD v4: 3-119413721-T-TAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413721_119413722insAGA , CM000665.2:g.119413721_119413722insAGA	GRCh38
NC_000003.11:g.119132568_119132569insAGA , CM000665.1:g.119132568_119132569insAGA	GRCh37
NC_000003.10:g.120615258_120615259insAGA	NCBI36
NG_007665.2:g.124349_124350insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1927-135_1927-134insAGA MANE Select	ENSP00000264245.4:n.1927-135_1927-134insAGA
ENST00000264245.8:c.1927-135_1927-134insAGA	ENSP00000264245.4:n.1927-135_1927-134insAGA
NM_020754.3:c.1927-135_1927-134insAGA	NP_065805.2:n.1927-135_1927-134insAGA
XM_005247671.3:c.1834-135_1834-134insAGA	XP_005247728.1:n.1834-135_1834-134insAGA
XM_006713714.2:c.1867-135_1867-134insAGA	XP_006713777.1:n.1867-135_1867-134insAGA
XM_006713714.3:c.1867-135_1867-134insAGA	XP_006713777.1:n.1867-135_1867-134insAGA
XM_017006955.1:c.1435-135_1435-134insAGA	XP_016862444.1:n.1435-135_1435-134insAGA
NM_020754.4:c.1927-135_1927-134insAGA MANE Select	NP_065805.2:n.1927-135_1927-134insAGA