Canonical Allele Identifier: CA2618599574

Gene: WNT1

Linked Data

• gnomAD v4: 12-48981559-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48981560del , CM000674.2:g.48981560del	GRCh38
NC_000012.11:g.49375343del , CM000674.1:g.49375343del	GRCh37
NC_000012.10:g.47661610del	NCBI36
NG_033141.1:g.8108del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293549.4:c.1033del MANE Select	ENSP00000293549.3:p.Cys345AlafsTer?
ENST00000293549.3:c.1033del	ENSP00000293549.3:p.Cys345AlafsTer?
ENST00000613114.4:c.1000del	ENSP00000481240.1:p.Cys334AlafsTer?
NM_005430.3:c.1033del	NP_005421.1:p.Cys345AlafsTer?
NM_005430.4:c.1033del MANE Select	NP_005421.1:p.Cys345AlafsTer?