Canonical Allele Identifier: CA1428758864
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190404349_190404350delinsAT , CM000665.2:g.190404349_190404350delinsAT GRCh38
NC_000003.11:g.190122138_190122139delinsAT , CM000665.1:g.190122138_190122139delinsAT GRCh37
NC_000003.10:g.191604832_191604833delinsAT NCBI36
NG_008149.1:g.21298_21299delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.218-413_218-412delinsAT MANE Select ENSP00000264734.3:n.218-413_218-412delinsAT
ENST00000456423.2:c.115-5554_115-5553delinsAT ENSP00000414136.2:n.115-5554_115-5553delinsAT
ENST00000264734.2:c.428-413_428-412delinsAT ENSP00000264734.2:n.428-413_428-412delinsAT
ENST00000456423.1:c.325-5554_325-5553delinsAT ENSP00000414136.1:n.325-5554_325-5553delinsAT
ENST00000468220.1:n.410-413_410-412delinsAT
NM_006580.3:c.428-413_428-412delinsAT NP_006571.1:n.428-413_428-412delinsAT
NM_001378492.1:c.218-413_218-412delinsAT NP_001365421.1:n.218-413_218-412delinsAT
NM_001378493.1:c.218-413_218-412delinsAT NP_001365422.1:n.218-413_218-412delinsAT
NM_006580.4:c.218-413_218-412delinsAT MANE Select NP_006571.2:n.218-413_218-412delinsAT