Canonical Allele Identifier: CA479704598

Gene: WNT1

Linked Data

• MyVariant Identifiers: chr12:g.49375402C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48981619C>G , CM000674.2:g.48981619C>G	GRCh38
NC_000012.11:g.49375402C>G , CM000674.1:g.49375402C>G	GRCh37
NC_000012.10:g.47661669C>G	NCBI36
NG_033141.1:g.8167C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293549.4:c.1092C>G MANE Select	ENSP00000293549.3:p.Arg364=
ENST00000293549.3:c.1092C>G	ENSP00000293549.3:p.Arg364=
ENST00000613114.4:c.1059C>G	ENSP00000481240.1:p.Arg353=
NM_005430.3:c.1092C>G	NP_005421.1:p.Arg364=
NM_005430.4:c.1092C>G MANE Select	NP_005421.1:p.Arg364=