Canonical Allele Identifier: CA689545061
Gene: WNT1 HGNC NCBI

Linked Data

dbSNP Id: rs1366288205
MyVariant Identifiers: chr12:g.49375569_49375571del (hg19) chr12:g.48981786_48981788del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981790_48981792del , CM000674.2:g.48981790_48981792del GRCh38
NC_000012.11:g.49375573_49375575del , CM000674.1:g.49375573_49375575del GRCh37
NC_000012.10:g.47661840_47661842del NCBI36
NG_033141.1:g.8338_8340del

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*150_*152del MANE Select ENSP00000293549.3:n.*150_*152del
NM_005430.3:c.*150_*152del NP_005421.1:n.*150_*152del
NM_005430.4:c.*150_*152del MANE Select NP_005421.1:n.*150_*152del
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