Canonical Allele Identifier: CA2034926087
Gene: WNT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981385C= , CM000674.2:g.48981385C= GRCh38
NC_000012.11:g.49375168C= , CM000674.1:g.49375168C= GRCh37
NC_000012.10:g.47661435C= NCBI36
NG_033141.1:g.7933C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.858C= MANE Select ENSP00000293549.3:p.Pro286=
ENST00000293549.3:c.858C= ENSP00000293549.3:p.Pro286=
ENST00000613114.4:c.828-3C= ENSP00000481240.1:n.828-3C=
NM_005430.3:c.858C= NP_005421.1:p.Pro286=
NM_005430.4:c.858C= MANE Select NP_005421.1:p.Pro286=
Search 100 bp 5'
Search 100 bp 3'