Canonical Allele Identifier: CA2669041729
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408303del , CM000665.2:g.190408303del GRCh38
NC_000003.11:g.190126092del , CM000665.1:g.190126092del GRCh37
NC_000003.10:g.191608786del NCBI36
NG_008149.1:g.25252del

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.383-11del MANE Select ENSP00000264734.3:n.383-11del
ENST00000456423.2:c.115-1600del ENSP00000414136.2:n.115-1600del
ENST00000264734.2:c.593-11del ENSP00000264734.2:n.593-11del
ENST00000456423.1:c.325-1600del ENSP00000414136.1:n.325-1600del
NM_006580.3:c.593-11del NP_006571.1:n.593-11del
NM_001378492.1:c.383-11del NP_001365421.1:n.383-11del
NM_001378493.1:c.383-11del NP_001365422.1:n.383-11del
NM_006580.4:c.383-11del MANE Select NP_006571.2:n.383-11del