Canonical Allele Identifier: CA384638764
Gene: WNT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981572T>A , CM000674.2:g.48981572T>A GRCh38
NC_000012.11:g.49375355T>A , CM000674.1:g.49375355T>A GRCh37
NC_000012.10:g.47661622T>A NCBI36
NG_033141.1:g.8120T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.1045T>A MANE Select ENSP00000293549.3:p.Phe349Ile
ENST00000293549.3:c.1045T>A ENSP00000293549.3:p.Phe349Ile
ENST00000613114.4:c.1012T>A ENSP00000481240.1:p.Phe338Ile
NM_005430.3:c.1045T>A NP_005421.1:p.Phe349Ile
NM_005430.4:c.1045T>A MANE Select NP_005421.1:p.Phe349Ile