Canonical Allele Identifier: CA384638775
Gene: WNT1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.1045T>G MANE Select ENSP00000293549.3:p.Phe349Val
ENST00000293549.3:c.1045T>G ENSP00000293549.3:p.Phe349Val
ENST00000613114.4:c.1012T>G ENSP00000481240.1:p.Phe338Val
NM_005430.3:c.1045T>G NP_005421.1:p.Phe349Val
NM_005430.4:c.1045T>G MANE Select NP_005421.1:p.Phe349Val