ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA355762123
Gene: CLDN16
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr3:g.190105921A>C (hg19)
chr3:g.190388132A>C (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.190388132A>C , CM000665.2:g.190388132A>C
GRCh38
NC_000003.11:g.190105921A>C , CM000665.1:g.190105921A>C
GRCh37
NC_000003.10:g.191588615A>C
NCBI36
NG_008149.1:g.5081A>C
Transcript Alleles
HGVS
Amino-acid Change
ENST00000456423.2:c.-198A>C
ENSP00000414136.2:n.-198A>C
ENST00000264734.2:c.13A>C
ENSP00000264734.2:p.Thr5Pro
ENST00000456423.1:c.13A>C
ENSP00000414136.1:p.Thr5Pro
ENST00000468220.1:n.306+13529A>C
NM_006580.3:c.13A>C
NP_006571.1:p.Thr5Pro
NM_001378492.1:c.-93-105A>C
NP_001365421.1:n.-93-105A>C
NM_001378493.1:c.-93-105A>C
NP_001365422.1:n.-93-105A>C
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