Canonical Allele Identifier: CA2663174719
Gene: WNT10A HGNC NCBI

Linked Data

gnomAD v4: 2-218893423-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893423T>C , CM000664.2:g.218893423T>C GRCh38
NC_000002.11:g.219758145T>C , CM000664.1:g.219758145T>C GRCh37
NC_000002.10:g.219466389T>C NCBI36
NG_012179.1:g.17891T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.*152T>C MANE Select ENSP00000258411.3:n.*152T>C
ENST00000258411.7:c.*152T>C ENSP00000258411.3:n.*152T>C
ENST00000489887.1:n.47+156T>C
NM_025216.2:c.*152T>C NP_079492.2:n.*152T>C
XM_011511928.1:c.*152T>C XP_011510230.1:n.*152T>C
XM_011511929.1:c.*152T>C XP_011510231.1:n.*152T>C
XM_011511930.1:c.*126T>C XP_011510232.1:n.*126T>C
XM_011511929.2:c.*152T>C XP_011510231.1:n.*152T>C
NM_025216.3:c.*152T>C MANE Select NP_079492.2:n.*152T>C
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