Canonical Allele Identifier: CA1428757298
Gene: CLDN16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190402606A= , CM000665.2:g.190402606A= GRCh38
NC_000003.11:g.190120395A= , CM000665.1:g.190120395A= GRCh37
NC_000003.10:g.191603089A= NCBI36
NG_008149.1:g.19555A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.217+167A= MANE Select ENSP00000264734.3:n.217+167A=
ENST00000456423.2:c.115-7297A= ENSP00000414136.2:n.115-7297A=
ENST00000264734.2:c.427+167A= ENSP00000264734.2:n.427+167A=
ENST00000456423.1:c.325-7297A= ENSP00000414136.1:n.325-7297A=
ENST00000468220.1:n.409+167A=
NM_006580.3:c.427+167A= NP_006571.1:n.427+167A=
NM_001378492.1:c.217+167A= NP_001365421.1:n.217+167A=
NM_001378493.1:c.217+167A= NP_001365422.1:n.217+167A=
NM_006580.4:c.217+167A= MANE Select NP_006571.2:n.217+167A=
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