Canonical Allele Identifier: CA2034902077
Gene: WNT1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981530C= , CM000674.2:g.48981530C= GRCh38
NC_000012.11:g.49375313C= , CM000674.1:g.49375313C= GRCh37
NC_000012.10:g.47661580C= NCBI36
NG_033141.1:g.8078C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.1003C= MANE Select ENSP00000293549.3:p.Arg335=
ENST00000293549.3:c.1003C= ENSP00000293549.3:p.Arg335=
ENST00000613114.4:c.970C= ENSP00000481240.1:p.Arg324=
NM_005430.3:c.1003C= NP_005421.1:p.Arg335=
NM_005430.4:c.1003C= MANE Select NP_005421.1:p.Arg335=
Search 100 bp 5'
Search 100 bp 3'