Canonical Allele Identifier: CA2034902103
Gene: WNT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981586_48981588delinsCCA , CM000674.2:g.48981586_48981588delinsCCA GRCh38
NC_000012.11:g.49375369_49375371delinsCCA , CM000674.1:g.49375369_49375371delinsCCA GRCh37
NC_000012.10:g.47661636_47661638delinsCCA NCBI36
NG_033141.1:g.8134_8136delinsCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.1059_1061delinsCCA MANE Select ENSP00000293549.3:p.Cys353=
ENST00000293549.3:c.1059_1061delinsCCA ENSP00000293549.3:p.Cys353=
ENST00000613114.4:c.1026_1028delinsCCA ENSP00000481240.1:p.Cys342=
NM_005430.3:c.1059_1061delinsCCA NP_005421.1:p.Cys353=
NM_005430.4:c.1059_1061delinsCCA MANE Select NP_005421.1:p.Cys353=
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