Canonical Allele Identifier: CA355762219
Gene: CLDN16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.190105965C>G (hg19) chr3:g.190388176C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388176C>G , CM000665.2:g.190388176C>G GRCh38
NC_000003.11:g.190105965C>G , CM000665.1:g.190105965C>G GRCh37
NC_000003.10:g.191588659C>G NCBI36
NG_008149.1:g.5125C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.-154C>G MANE Select ENSP00000264734.3:n.-154C>G
ENST00000456423.2:c.-154C>G ENSP00000414136.2:n.-154C>G
ENST00000264734.2:c.57C>G ENSP00000264734.2:p.Asn19Lys
ENST00000456423.1:c.57C>G ENSP00000414136.1:p.Asn19Lys
ENST00000468220.1:n.306+13573C>G
NM_006580.3:c.57C>G NP_006571.1:p.Asn19Lys
NM_001378492.1:c.-93-61C>G NP_001365421.1:n.-93-61C>G
NM_001378493.1:c.-93-61C>G NP_001365422.1:n.-93-61C>G
NM_006580.4:c.-154C>G MANE Select NP_006571.2:n.-154C>G
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