Canonical Allele Identifier: CA384637314
Gene: WNT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981462G>A , CM000674.2:g.48981462G>A GRCh38
NC_000012.11:g.49375245G>A , CM000674.1:g.49375245G>A GRCh37
NC_000012.10:g.47661512G>A NCBI36
NG_033141.1:g.8010G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.935G>A MANE Select ENSP00000293549.3:p.Gly312Glu
ENST00000293549.3:c.935G>A ENSP00000293549.3:p.Gly312Glu
ENST00000613114.4:c.902G>A ENSP00000481240.1:p.Gly301Glu
NM_005430.3:c.935G>A NP_005421.1:p.Gly312Glu
NM_005430.4:c.935G>A MANE Select NP_005421.1:p.Gly312Glu