Canonical Allele Identifier: CA2034902133
Gene: WNT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981649G= , CM000674.2:g.48981649G= GRCh38
NC_000012.11:g.49375432G= , CM000674.1:g.49375432G= GRCh37
NC_000012.10:g.47661699G= NCBI36
NG_033141.1:g.8197G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*9G= MANE Select ENSP00000293549.3:n.*9G=
ENST00000293549.3:c.*9G= ENSP00000293549.3:n.*9G=
NM_005430.3:c.*9G= NP_005421.1:n.*9G=
NM_005430.4:c.*9G= MANE Select NP_005421.1:n.*9G=
Search 100 bp 5'
Search 100 bp 3'