Canonical Allele Identifier: CA914821012

Gene: ARHGAP31

Linked Data

• dbSNP Id: rs1559998131
• gnomAD v2: 3-119132599-T-TG
• gnomAD v3: 3-119413752-T-TG
• gnomAD v4: 3-119413752-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413754dup , CM000665.2:g.119413754dup	GRCh38
NC_000003.11:g.119132601dup , CM000665.1:g.119132601dup	GRCh37
NC_000003.10:g.120615291dup	NCBI36
NG_007665.2:g.124382dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1927-102dup MANE Select	ENSP00000264245.4:n.1927-102dup
ENST00000264245.8:c.1927-102dup	ENSP00000264245.4:n.1927-102dup
NM_020754.3:c.1927-102dup	NP_065805.2:n.1927-102dup
XM_005247671.3:c.1834-102dup	XP_005247728.1:n.1834-102dup
XM_006713714.2:c.1867-102dup	XP_006713777.1:n.1867-102dup
XM_006713714.3:c.1867-102dup	XP_006713777.1:n.1867-102dup
XM_017006955.1:c.1435-102dup	XP_016862444.1:n.1435-102dup
NM_020754.4:c.1927-102dup MANE Select	NP_065805.2:n.1927-102dup