Canonical Allele Identifier: CA1428775577
Gene: CLDN16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388128C= , CM000665.2:g.190388128C= GRCh38
NC_000003.11:g.190105917C= , CM000665.1:g.190105917C= GRCh37
NC_000003.10:g.191588611C= NCBI36
NG_008149.1:g.5077C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000456423.2:c.-202C= ENSP00000414136.2:n.-202C=
ENST00000264734.2:c.9C= ENSP00000264734.2:p.Ser3=
ENST00000456423.1:c.9C= ENSP00000414136.1:p.Ser3=
ENST00000468220.1:n.306+13525C=
NM_006580.3:c.9C= NP_006571.1:p.Ser3=
NM_001378492.1:c.-93-109C= NP_001365421.1:n.-93-109C=
NM_001378493.1:c.-93-109C= NP_001365422.1:n.-93-109C=
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