Canonical Allele Identifier: CA2034902145
Gene: WNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981666A= , CM000674.2:g.48981666A= GRCh38
NC_000012.11:g.49375449A= , CM000674.1:g.49375449A= GRCh37
NC_000012.10:g.47661716A= NCBI36
NG_033141.1:g.8214A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*26A= MANE Select ENSP00000293549.3:n.*26A=
ENST00000293549.3:c.*26A= ENSP00000293549.3:n.*26A=
NM_005430.3:c.*26A= NP_005421.1:n.*26A=
NM_005430.4:c.*26A= MANE Select NP_005421.1:n.*26A=