Canonical Allele Identifier: CA1139657706

Gene: WNT10A

Linked Data

• ClinVar Variation Id: 896531
• ClinVar RCV Id: RCV001139236 ; RCV001139234 ; RCV001139235
• dbSNP Id: rs1944681589
• gnomAD v4: 2-218893410-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893410C>G , CM000664.2:g.218893410C>G	GRCh38
NC_000002.11:g.219758132C>G , CM000664.1:g.219758132C>G	GRCh37
NC_000002.10:g.219466376C>G	NCBI36
NG_012179.1:g.17878C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.*139C>G MANE Select	ENSP00000258411.3:n.*139C>G
ENST00000258411.7:c.*139C>G	ENSP00000258411.3:n.*139C>G
ENST00000489887.1:n.47+143C>G
NM_025216.2:c.*139C>G	NP_079492.2:n.*139C>G
XM_011511928.1:c.*139C>G	XP_011510230.1:n.*139C>G
XM_011511929.1:c.*139C>G	XP_011510231.1:n.*139C>G
XM_011511930.1:c.*113C>G	XP_011510232.1:n.*113C>G
XM_011511929.2:c.*139C>G	XP_011510231.1:n.*139C>G
NM_025216.3:c.*139C>G MANE Select	NP_079492.2:n.*139C>G