Canonical Allele Identifier: CA545960946

Gene: ARHGAP31

Linked Data

• dbSNP Id: rs1213355358
• gnomAD v2: 3-119134039-T-TA
• gnomAD v4: 3-119415192-T-TA
• MyVariant Identifiers: chr3:g.119134039_119134040insA (hg19) ; chr3:g.119415192_119415193insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119415193dup , CM000665.2:g.119415193dup	GRCh38
NC_000003.11:g.119134040dup , CM000665.1:g.119134040dup	GRCh37
NC_000003.10:g.120616730dup	NCBI36
NG_007665.2:g.125821dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.3264dup MANE Select	ENSP00000264245.4:p.Gln1089ThrfsTer29
ENST00000264245.8:c.3264dup	ENSP00000264245.4:p.Gln1089ThrfsTer29
NM_020754.3:c.3264dup	NP_065805.2:p.Gln1089ThrfsTer29
XM_005247671.3:c.3171dup	XP_005247728.1:p.Gln1058ThrfsTer29
XM_006713714.2:c.3204dup	XP_006713777.1:p.Gln1069ThrfsTer29
XM_006713714.3:c.3204dup	XP_006713777.1:p.Gln1069ThrfsTer29
XM_017006955.1:c.2772dup	XP_016862444.1:p.Gln925ThrfsTer29
NM_020754.4:c.3264dup MANE Select	NP_065805.2:p.Gln1089ThrfsTer29