Canonical Allele Identifier: CA10617842
Gene: CLDN16 HGNC NCBI

Linked Data

ClinVar Variation Id: 344444
ClinVar RCV Id: RCV000285445
dbSNP Id: rs886058244
MyVariant Identifiers: chr3:g.190105946del (hg19) chr3:g.190388157del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388157del , CM000665.2:g.190388157del GRCh38
NC_000003.11:g.190105946del , CM000665.1:g.190105946del GRCh37
NC_000003.10:g.191588640del NCBI36
NG_008149.1:g.5106del

Transcript Alleles

HGVS Amino-acid Change
ENST00000456423.2:c.-173del ENSP00000414136.2:n.-173del
ENST00000264734.2:c.38del ENSP00000264734.2:p.Leu13CysfsTer15
ENST00000456423.1:c.38del ENSP00000414136.1:p.Leu13CysfsTer15
ENST00000468220.1:n.306+13554del
NM_006580.3:c.38del NP_006571.1:p.Leu13CysfsTer15
NM_001378492.1:c.-93-80del NP_001365421.1:n.-93-80del
NM_001378493.1:c.-93-80del NP_001365422.1:n.-93-80del
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