Canonical Allele Identifier: CA65850002

Gene: WNT10A

Linked Data

• dbSNP Id: rs1021375512
• gnomAD v2: 2-219746654-C-A
• gnomAD v3: 2-218881932-C-A
• gnomAD v4: 2-218881932-C-A
• MyVariant Identifiers: chr2:g.219746654C>A (hg19) ; chr2:g.218881932C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218881932C>A , CM000664.2:g.218881932C>A	GRCh38
NC_000002.11:g.219746654C>A , CM000664.1:g.219746654C>A	GRCh37
NC_000002.10:g.219454898C>A	NCBI36
NG_012179.1:g.6400C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000258411.8:c.114-229C>A MANE Select	ENSP00000258411.3:n.114-229C>A
ENST00000258411.7:c.114-229C>A	ENSP00000258411.3:n.114-229C>A
NM_025216.2:c.114-229C>A	NP_079492.2:n.114-229C>A
XM_011511928.1:c.63-229C>A	XP_011510230.1:n.63-229C>A
XM_011511929.1:c.18-229C>A	XP_011510231.1:n.18-229C>A
XM_011511930.1:c.114-229C>A	XP_011510232.1:n.114-229C>A
XM_011511929.2:c.18-229C>A	XP_011510231.1:n.18-229C>A
NM_025216.3:c.114-229C>A MANE Select	NP_079492.2:n.114-229C>A