Canonical Allele Identifier: CA1042495685
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs1944521192
gnomAD v3: 2-218881908-A-G
gnomAD v4: 2-218881908-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218881908A>G , CM000664.2:g.218881908A>G GRCh38
NC_000002.11:g.219746630A>G , CM000664.1:g.219746630A>G GRCh37
NC_000002.10:g.219454874A>G NCBI36
NG_012179.1:g.6376A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.114-253A>G MANE Select ENSP00000258411.3:n.114-253A>G
ENST00000258411.7:c.114-253A>G ENSP00000258411.3:n.114-253A>G
NM_025216.2:c.114-253A>G NP_079492.2:n.114-253A>G
XM_011511928.1:c.63-253A>G XP_011510230.1:n.63-253A>G
XM_011511929.1:c.18-253A>G XP_011510231.1:n.18-253A>G
XM_011511930.1:c.114-253A>G XP_011510232.1:n.114-253A>G
XM_011511929.2:c.18-253A>G XP_011510231.1:n.18-253A>G
NM_025216.3:c.114-253A>G MANE Select NP_079492.2:n.114-253A>G
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