Canonical Allele Identifier: CA384638691
Gene: WNT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981564A>T , CM000674.2:g.48981564A>T GRCh38
NC_000012.11:g.49375347A>T , CM000674.1:g.49375347A>T GRCh37
NC_000012.10:g.47661614A>T NCBI36
NG_033141.1:g.8112A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.1037A>T MANE Select ENSP00000293549.3:p.Asn346Ile
ENST00000293549.3:c.1037A>T ENSP00000293549.3:p.Asn346Ile
ENST00000613114.4:c.1004A>T ENSP00000481240.1:p.Asn335Ile
NM_005430.3:c.1037A>T NP_005421.1:p.Asn346Ile
NM_005430.4:c.1037A>T MANE Select NP_005421.1:p.Asn346Ile