Canonical Allele Identifier: CA764938547

Gene: WNT10A

Linked Data

• dbSNP Id: rs749297006
• gnomAD v3: 2-218882193-T-TC
• gnomAD v4: 2-218882193-T-TC
• MyVariant Identifiers: chr2:g.219746915_219746916insC (hg19) ; chr2:g.218882193_218882194insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882199dup , CM000664.2:g.218882199dup	GRCh38
NC_000002.11:g.219746921dup , CM000664.1:g.219746921dup	GRCh37
NC_000002.10:g.219455165dup	NCBI36
NG_012179.1:g.6667dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.152dup MANE Select	ENSP00000258411.3:p.Glu52GlyfsTer29
ENST00000258411.7:c.152dup	ENSP00000258411.3:p.Glu52GlyfsTer29
ENST00000458582.1:c.39dup
NM_025216.2:c.152dup	NP_079492.2:p.Glu52GlyfsTer29
XM_011511928.1:c.101dup	XP_011510230.1:p.Glu35GlyfsTer29
XM_011511929.1:c.56dup	XP_011510231.1:p.Glu20GlyfsTer29
XM_011511930.1:c.152dup	XP_011510232.1:p.Glu52GlyfsTer29
XM_011511929.2:c.56dup	XP_011510231.1:p.Glu20GlyfsTer29
NM_025216.3:c.152dup MANE Select	NP_079492.2:p.Glu52GlyfsTer29