Canonical Allele Identifier: CA384639136
Gene: WNT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981600G>C , CM000674.2:g.48981600G>C GRCh38
NC_000012.11:g.49375383G>C , CM000674.1:g.49375383G>C GRCh37
NC_000012.10:g.47661650G>C NCBI36
NG_033141.1:g.8148G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.1073G>C MANE Select ENSP00000293549.3:p.Arg358Pro
ENST00000293549.3:c.1073G>C ENSP00000293549.3:p.Arg358Pro
ENST00000613114.4:c.1040G>C ENSP00000481240.1:p.Arg347Pro
NM_005430.3:c.1073G>C NP_005421.1:p.Arg358Pro
NM_005430.4:c.1073G>C MANE Select NP_005421.1:p.Arg358Pro