Canonical Allele Identifier: CA1428775655
Gene: CLDN16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388173C= , CM000665.2:g.190388173C= GRCh38
NC_000003.11:g.190105962C= , CM000665.1:g.190105962C= GRCh37
NC_000003.10:g.191588656C= NCBI36
NG_008149.1:g.5122C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.-157C= MANE Select ENSP00000264734.3:n.-157C=
ENST00000456423.2:c.-157C= ENSP00000414136.2:n.-157C=
ENST00000264734.2:c.54C= ENSP00000264734.2:p.Cys18=
ENST00000456423.1:c.54C= ENSP00000414136.1:p.Cys18=
ENST00000468220.1:n.306+13570C=
NM_006580.3:c.54C= NP_006571.1:p.Cys18=
NM_001378492.1:c.-93-64C= NP_001365421.1:n.-93-64C=
NM_001378493.1:c.-93-64C= NP_001365422.1:n.-93-64C=
NM_006580.4:c.-157C= MANE Select NP_006571.2:n.-157C=
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