Canonical Allele Identifier: CA914821013

Gene: ARHGAP31

Linked Data

• dbSNP Id: rs1559998135
• gnomAD v2: 3-119132602-C-CTG
• gnomAD v3: 3-119413755-C-CTG
• gnomAD v4: 3-119413755-C-CTG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413755_119413756insTG , CM000665.2:g.119413755_119413756insTG	GRCh38
NC_000003.11:g.119132602_119132603insTG , CM000665.1:g.119132602_119132603insTG	GRCh37
NC_000003.10:g.120615292_120615293insTG	NCBI36
NG_007665.2:g.124383_124384insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1927-101_1927-100insTG MANE Select	ENSP00000264245.4:n.1927-101_1927-100insTG
ENST00000264245.8:c.1927-101_1927-100insTG	ENSP00000264245.4:n.1927-101_1927-100insTG
NM_020754.3:c.1927-101_1927-100insTG	NP_065805.2:n.1927-101_1927-100insTG
XM_005247671.3:c.1834-101_1834-100insTG	XP_005247728.1:n.1834-101_1834-100insTG
XM_006713714.2:c.1867-101_1867-100insTG	XP_006713777.1:n.1867-101_1867-100insTG
XM_006713714.3:c.1867-101_1867-100insTG	XP_006713777.1:n.1867-101_1867-100insTG
XM_017006955.1:c.1435-101_1435-100insTG	XP_016862444.1:n.1435-101_1435-100insTG
NM_020754.4:c.1927-101_1927-100insTG MANE Select	NP_065805.2:n.1927-101_1927-100insTG