Canonical Allele Identifier: CA355762655
Gene: CLDN16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.190106174T>C (hg19) chr3:g.190388385T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388385T>C , CM000665.2:g.190388385T>C GRCh38
NC_000003.11:g.190106174T>C , CM000665.1:g.190106174T>C GRCh37
NC_000003.10:g.191588868T>C NCBI36
NG_008149.1:g.5334T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.56T>C MANE Select ENSP00000264734.3:p.Phe19Ser
ENST00000456423.2:c.56T>C ENSP00000414136.2:p.Phe19Ser
ENST00000264734.2:c.266T>C ENSP00000264734.2:p.Phe89Ser
ENST00000456423.1:c.266T>C ENSP00000414136.1:p.Phe89Ser
ENST00000468220.1:n.306+13782T>C
NM_006580.3:c.266T>C NP_006571.1:p.Phe89Ser
NM_001378492.1:c.56T>C NP_001365421.1:p.Phe19Ser
NM_001378493.1:c.56T>C NP_001365422.1:p.Phe19Ser
NM_006580.4:c.56T>C MANE Select NP_006571.2:p.Phe19Ser
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