Canonical Allele Identifier: CA1428775748
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388233C= , CM000665.2:g.190388233C= GRCh38
NC_000003.11:g.190106022C= , CM000665.1:g.190106022C= GRCh37
NC_000003.10:g.191588716C= NCBI36
NG_008149.1:g.5182C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.-97C= MANE Select ENSP00000264734.3:n.-97C=
ENST00000456423.2:c.-97C= ENSP00000414136.2:n.-97C=
ENST00000264734.2:c.114C= ENSP00000264734.2:p.Cys38=
ENST00000456423.1:c.114C= ENSP00000414136.1:p.Cys38=
ENST00000468220.1:n.306+13630C=
NM_006580.3:c.114C= NP_006571.1:p.Cys38=
NM_001378492.1:c.-93-4C= NP_001365421.1:n.-93-4C=
NM_001378493.1:c.-93-4C= NP_001365422.1:n.-93-4C=
NM_006580.4:c.-97C= MANE Select NP_006571.2:n.-97C=