Canonical Allele Identifier: CA384638758

Gene: WNT1

Linked Data

• MyVariant Identifiers: chr12:g.49375353C>G (hg19) ; chr12:g.48981570C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48981570C>G , CM000674.2:g.48981570C>G	GRCh38
NC_000012.11:g.49375353C>G , CM000674.1:g.49375353C>G	GRCh37
NC_000012.10:g.47661620C>G	NCBI36
NG_033141.1:g.8118C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293549.4:c.1043C>G MANE Select	ENSP00000293549.3:p.Thr348Ser
ENST00000293549.3:c.1043C>G	ENSP00000293549.3:p.Thr348Ser
ENST00000613114.4:c.1010C>G	ENSP00000481240.1:p.Thr337Ser
NM_005430.3:c.1043C>G	NP_005421.1:p.Thr348Ser
NM_005430.4:c.1043C>G MANE Select	NP_005421.1:p.Thr348Ser