Canonical Allele Identifier: CA658797896

Gene: WNT1

Linked Data

• ClinVar Variation Id: 524168
• ClinVar RCV Id: RCV000627667
• dbSNP Id: rs1555179156

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48981587_48981588delinsG , CM000674.2:g.48981587_48981588delinsG	GRCh38
NC_000012.11:g.49375370_49375371delinsG , CM000674.1:g.49375370_49375371delinsG	GRCh37
NC_000012.10:g.47661637_47661638delinsG	NCBI36
NG_033141.1:g.8135_8136delinsG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293549.4:c.1060_1061delinsG MANE Select	ENSP00000293549.3:p.His354AlafsTer?
ENST00000293549.3:c.1060_1061delinsG	ENSP00000293549.3:p.His354AlafsTer?
ENST00000613114.4:c.1027_1028delinsG	ENSP00000481240.1:p.His343AlafsTer?
NM_005430.3:c.1060_1061delinsG	NP_005421.1:p.His354AlafsTer?
NM_005430.4:c.1060_1061delinsG MANE Select	NP_005421.1:p.His354AlafsTer?