Canonical Allele Identifier: CA384639014
Gene: WNT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2692186
ClinVar RCV Id: RCV003494383

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981586C>G , CM000674.2:g.48981586C>G GRCh38
NC_000012.11:g.49375369C>G , CM000674.1:g.49375369C>G GRCh37
NC_000012.10:g.47661636C>G NCBI36
NG_033141.1:g.8134C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.1059C>G MANE Select ENSP00000293549.3:p.Cys353Trp
ENST00000293549.3:c.1059C>G ENSP00000293549.3:p.Cys353Trp
ENST00000613114.4:c.1026C>G ENSP00000481240.1:p.Cys342Trp
NM_005430.3:c.1059C>G NP_005421.1:p.Cys353Trp
NM_005430.4:c.1059C>G MANE Select NP_005421.1:p.Cys353Trp