Canonical Allele Identifier: CA2113848
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs760413231
ExAC: 2:219746922 G / A
gnomAD v2: 2-219746922-G-A
gnomAD v3: 2-218882200-G-A
gnomAD v4: 2-218882200-G-A
MyVariant Identifiers: chr2:g.219746922G>A (hg19) chr2:g.218882200G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882200G>A , CM000664.2:g.218882200G>A GRCh38
NC_000002.11:g.219746922G>A , CM000664.1:g.219746922G>A GRCh37
NC_000002.10:g.219455166G>A NCBI36
NG_012179.1:g.6668G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.153G>A MANE Select ENSP00000258411.3:p.Pro51=
ENST00000258411.7:c.153G>A ENSP00000258411.3:p.Pro51=
ENST00000458582.1:c.40G>A
NM_025216.2:c.153G>A NP_079492.2:p.Pro51=
XM_011511928.1:c.102G>A XP_011510230.1:p.Pro34=
XM_011511929.1:c.57G>A XP_011510231.1:p.Pro19=
XM_011511930.1:c.153G>A XP_011510232.1:p.Pro51=
XM_011511929.2:c.57G>A XP_011510231.1:p.Pro19=
NM_025216.3:c.153G>A MANE Select NP_079492.2:p.Pro51=
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Search 100 bp 3'