Canonical Allele Identifier: CA2759869859
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190402573_190402574insGACCGAACCTTAATAT , CM000665.2:g.190402573_190402574insGACCGAACCTTAATAT GRCh38
NC_000003.11:g.190120362_190120363insGACCGAACCTTAATAT , CM000665.1:g.190120362_190120363insGACCGAACCTTAATAT GRCh37
NC_000003.10:g.191603056_191603057insGACCGAACCTTAATAT NCBI36
NG_008149.1:g.19522_19523insGACCGAACCTTAATAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.217+134_217+135insGACCGAACCTTAATAT MANE Select ENSP00000264734.3:n.217+134_217+135insGACCGAACCTTAATAT
ENST00000456423.2:c.115-7330_115-7329insGACCGAACCTTAATAT ENSP00000414136.2:n.115-7330_115-7329insGACCGAACCTTAATAT
ENST00000264734.2:c.427+134_427+135insGACCGAACCTTAATAT ENSP00000264734.2:n.427+134_427+135insGACCGAACCTTAATAT
ENST00000456423.1:c.325-7330_325-7329insGACCGAACCTTAATAT ENSP00000414136.1:n.325-7330_325-7329insGACCGAACCTTAATAT
ENST00000468220.1:n.409+134_409+135insGACCGAACCTTAATAT
NM_006580.3:c.427+134_427+135insGACCGAACCTTAATAT NP_006571.1:n.427+134_427+135insGACCGAACCTTAATAT
NM_001378492.1:c.217+134_217+135insGACCGAACCTTAATAT NP_001365421.1:n.217+134_217+135insGACCGAACCTTAATAT
NM_001378493.1:c.217+134_217+135insGACCGAACCTTAATAT NP_001365422.1:n.217+134_217+135insGACCGAACCTTAATAT
NM_006580.4:c.217+134_217+135insGACCGAACCTTAATAT MANE Select NP_006571.2:n.217+134_217+135insGACCGAACCTTAATAT