Canonical Allele Identifier: CA2667110266

Gene: ARHGAP31

Linked Data

• gnomAD v4: 3-119413847-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413852dup , CM000665.2:g.119413852dup	GRCh38
NC_000003.11:g.119132699dup , CM000665.1:g.119132699dup	GRCh37
NC_000003.10:g.120615389dup	NCBI36
NG_007665.2:g.124480dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1927-4dup MANE Select	ENSP00000264245.4:n.1927-4dup
ENST00000264245.8:c.1927-4dup	ENSP00000264245.4:n.1927-4dup
NM_020754.3:c.1927-4dup	NP_065805.2:n.1927-4dup
XM_005247671.3:c.1834-4dup	XP_005247728.1:n.1834-4dup
XM_006713714.2:c.1867-4dup	XP_006713777.1:n.1867-4dup
XM_006713714.3:c.1867-4dup	XP_006713777.1:n.1867-4dup
XM_017006955.1:c.1435-4dup	XP_016862444.1:n.1435-4dup
NM_020754.4:c.1927-4dup MANE Select	NP_065805.2:n.1927-4dup