Canonical Allele Identifier: CA2034926169
Gene: WNT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981448A= , CM000674.2:g.48981448A= GRCh38
NC_000012.11:g.49375231A= , CM000674.1:g.49375231A= GRCh37
NC_000012.10:g.47661498A= NCBI36
NG_033141.1:g.7996A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.921A= MANE Select ENSP00000293549.3:p.Thr307=
ENST00000293549.3:c.921A= ENSP00000293549.3:p.Thr307=
ENST00000613114.4:c.888A= ENSP00000481240.1:p.Thr296=
NM_005430.3:c.921A= NP_005421.1:p.Thr307=
NM_005430.4:c.921A= MANE Select NP_005421.1:p.Thr307=
Search 100 bp 5'
Search 100 bp 3'