Canonical Allele Identifier: CA1428759182
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190404696T= , CM000665.2:g.190404696T= GRCh38
NC_000003.11:g.190122485T= , CM000665.1:g.190122485T= GRCh37
NC_000003.10:g.191605179T= NCBI36
NG_008149.1:g.21645T=

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.218-66T= MANE Select ENSP00000264734.3:n.218-66T=
ENST00000456423.2:c.115-5207T= ENSP00000414136.2:n.115-5207T=
ENST00000264734.2:c.428-66T= ENSP00000264734.2:n.428-66T=
ENST00000456423.1:c.325-5207T= ENSP00000414136.1:n.325-5207T=
ENST00000468220.1:n.410-66T=
NM_006580.3:c.428-66T= NP_006571.1:n.428-66T=
NM_001378492.1:c.218-66T= NP_001365421.1:n.218-66T=
NM_001378493.1:c.218-66T= NP_001365422.1:n.218-66T=
NM_006580.4:c.218-66T= MANE Select NP_006571.2:n.218-66T=