Canonical Allele Identifier: CA1428775640
Gene: CLDN16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388166C= , CM000665.2:g.190388166C= GRCh38
NC_000003.11:g.190105955C= , CM000665.1:g.190105955C= GRCh37
NC_000003.10:g.191588649C= NCBI36
NG_008149.1:g.5115C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.-164C= MANE Select ENSP00000264734.3:n.-164C=
ENST00000456423.2:c.-164C= ENSP00000414136.2:n.-164C=
ENST00000264734.2:c.47C= ENSP00000264734.2:p.Ser16=
ENST00000456423.1:c.47C= ENSP00000414136.1:p.Ser16=
ENST00000468220.1:n.306+13563C=
NM_006580.3:c.47C= NP_006571.1:p.Ser16=
NM_001378492.1:c.-93-71C= NP_001365421.1:n.-93-71C=
NM_001378493.1:c.-93-71C= NP_001365422.1:n.-93-71C=
NM_006580.4:c.-164C= MANE Select NP_006571.2:n.-164C=
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