Canonical Allele Identifier: CA2663174712
Gene: WNT10A HGNC NCBI

Linked Data

gnomAD v4: 2-218893416-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893416T>G , CM000664.2:g.218893416T>G GRCh38
NC_000002.11:g.219758138T>G , CM000664.1:g.219758138T>G GRCh37
NC_000002.10:g.219466382T>G NCBI36
NG_012179.1:g.17884T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.*145T>G MANE Select ENSP00000258411.3:n.*145T>G
ENST00000258411.7:c.*145T>G ENSP00000258411.3:n.*145T>G
ENST00000489887.1:n.47+149T>G
NM_025216.2:c.*145T>G NP_079492.2:n.*145T>G
XM_011511928.1:c.*145T>G XP_011510230.1:n.*145T>G
XM_011511929.1:c.*145T>G XP_011510231.1:n.*145T>G
XM_011511930.1:c.*119T>G XP_011510232.1:n.*119T>G
XM_011511929.2:c.*145T>G XP_011510231.1:n.*145T>G
NM_025216.3:c.*145T>G MANE Select NP_079492.2:n.*145T>G
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