Canonical Allele Identifier: CA384638793
Gene: WNT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.49375356T>G (hg19) chr12:g.48981573T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981573T>G , CM000674.2:g.48981573T>G GRCh38
NC_000012.11:g.49375356T>G , CM000674.1:g.49375356T>G GRCh37
NC_000012.10:g.47661623T>G NCBI36
NG_033141.1:g.8121T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.1046T>G MANE Select ENSP00000293549.3:p.Phe349Cys
ENST00000293549.3:c.1046T>G ENSP00000293549.3:p.Phe349Cys
ENST00000613114.4:c.1013T>G ENSP00000481240.1:p.Phe338Cys
NM_005430.3:c.1046T>G NP_005421.1:p.Phe349Cys
NM_005430.4:c.1046T>G MANE Select NP_005421.1:p.Phe349Cys
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