Canonical Allele Identifier: CA1428756665
Gene: CLDN16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190402116C= , CM000665.2:g.190402116C= GRCh38
NC_000003.11:g.190119905C= , CM000665.1:g.190119905C= GRCh37
NC_000003.10:g.191602599C= NCBI36
NG_008149.1:g.19065C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.115-221C= MANE Select ENSP00000264734.3:n.115-221C=
ENST00000456423.2:c.115-7787C= ENSP00000414136.2:n.115-7787C=
ENST00000264734.2:c.325-221C= ENSP00000264734.2:n.325-221C=
ENST00000456423.1:c.325-7787C= ENSP00000414136.1:n.325-7787C=
ENST00000468220.1:n.307-221C=
NM_006580.3:c.325-221C= NP_006571.1:n.325-221C=
NM_001378492.1:c.115-221C= NP_001365421.1:n.115-221C=
NM_001378493.1:c.115-221C= NP_001365422.1:n.115-221C=
NM_006580.4:c.115-221C= MANE Select NP_006571.2:n.115-221C=
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