Canonical Allele Identifier: CA2034902119
Gene: WNT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981622A= , CM000674.2:g.48981622A= GRCh38
NC_000012.11:g.49375405A= , CM000674.1:g.49375405A= GRCh37
NC_000012.10:g.47661672A= NCBI36
NG_033141.1:g.8170A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.1095A= MANE Select ENSP00000293549.3:p.Val365=
ENST00000293549.3:c.1095A= ENSP00000293549.3:p.Val365=
ENST00000613114.4:c.1062A= ENSP00000481240.1:p.Val354=
NM_005430.3:c.1095A= NP_005421.1:p.Val365=
NM_005430.4:c.1095A= MANE Select NP_005421.1:p.Val365=
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