Canonical Allele Identifier: CA689545058

Gene: WNT1

Linked Data

• dbSNP Id: rs1315878263
• gnomAD v3: 12-48981779-TC-T
• gnomAD v4: 12-48981779-TC-T
• MyVariant Identifiers: chr12:g.49375563del (hg19) ; chr12:g.48981780del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48981782del , CM000674.2:g.48981782del	GRCh38
NC_000012.11:g.49375565del , CM000674.1:g.49375565del	GRCh37
NC_000012.10:g.47661832del	NCBI36
NG_033141.1:g.8330del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293549.4:c.*142del MANE Select	ENSP00000293549.3:n.*142del
NM_005430.3:c.*142del	NP_005421.1:n.*142del
NM_005430.4:c.*142del MANE Select	NP_005421.1:n.*142del