Canonical Allele Identifier: CA2034902124
Gene: WNT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981633G= , CM000674.2:g.48981633G= GRCh38
NC_000012.11:g.49375416G= , CM000674.1:g.49375416G= GRCh37
NC_000012.10:g.47661683G= NCBI36
NG_033141.1:g.8181G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.1106G= MANE Select ENSP00000293549.3:p.Cys369=
ENST00000293549.3:c.1106G= ENSP00000293549.3:p.Cys369=
ENST00000613114.4:c.1073G= ENSP00000481240.1:p.Cys358=
NM_005430.3:c.1106G= NP_005421.1:p.Cys369=
NM_005430.4:c.1106G= MANE Select NP_005421.1:p.Cys369=
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