Canonical Allele Identifier: CA384637284
Gene: WNT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981456C>G , CM000674.2:g.48981456C>G GRCh38
NC_000012.11:g.49375239C>G , CM000674.1:g.49375239C>G GRCh37
NC_000012.10:g.47661506C>G NCBI36
NG_033141.1:g.8004C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.929C>G MANE Select ENSP00000293549.3:p.Thr310Arg
ENST00000293549.3:c.929C>G ENSP00000293549.3:p.Thr310Arg
ENST00000613114.4:c.896C>G ENSP00000481240.1:p.Thr299Arg
NM_005430.3:c.929C>G NP_005421.1:p.Thr310Arg
NM_005430.4:c.929C>G MANE Select NP_005421.1:p.Thr310Arg