Canonical Allele Identifier: CA6544508
Gene: WNT1 HGNC NCBI

Linked Data

dbSNP Id: rs754821470
ExAC: 12:49375471 CCAAA / C
gnomAD v2: 12-49375471-CCAAA-C
gnomAD v3: 12-48981688-CCAAA-C
gnomAD v4: 12-48981688-CCAAA-C
MyVariant Identifiers: chr12:g.49375472_49375475del (hg19) chr12:g.48981689_48981692del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981691_48981694del , CM000674.2:g.48981691_48981694del GRCh38
NC_000012.11:g.49375474_49375477del , CM000674.1:g.49375474_49375477del GRCh37
NC_000012.10:g.47661741_47661744del NCBI36
NG_033141.1:g.8239_8242del

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*51_*54del MANE Select ENSP00000293549.3:n.*51_*54del
NM_005430.3:c.*51_*54del NP_005421.1:n.*51_*54del
NM_005430.4:c.*51_*54del MANE Select NP_005421.1:n.*51_*54del
Search 100 bp 5'
Search 100 bp 3'