Canonical Allele Identifier: CA1428762510
Gene: CLDN16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408171C= , CM000665.2:g.190408171C= GRCh38
NC_000003.11:g.190125960C= , CM000665.1:g.190125960C= GRCh37
NC_000003.10:g.191608654C= NCBI36
NG_008149.1:g.25120C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.383-143C= MANE Select ENSP00000264734.3:n.383-143C=
ENST00000456423.2:c.115-1732C= ENSP00000414136.2:n.115-1732C=
ENST00000264734.2:c.593-143C= ENSP00000264734.2:n.593-143C=
ENST00000456423.1:c.325-1732C= ENSP00000414136.1:n.325-1732C=
NM_006580.3:c.593-143C= NP_006571.1:n.593-143C=
NM_001378492.1:c.383-143C= NP_001365421.1:n.383-143C=
NM_001378493.1:c.383-143C= NP_001365422.1:n.383-143C=
NM_006580.4:c.383-143C= MANE Select NP_006571.2:n.383-143C=
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