Canonical Allele Identifier: CA2669054054
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190387986del , CM000665.2:g.190387986del GRCh38
NC_000003.11:g.190105775del , CM000665.1:g.190105775del GRCh37
NC_000003.10:g.191588469del NCBI36
NG_008149.1:g.4935del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-134del ENSP00000264734.2:n.-134del
ENST00000468220.1:n.306+13383del
NM_006580.3:c.-134del NP_006571.1:n.-134del
NM_001378492.1:c.-93-251del NP_001365421.1:n.-93-251del
NM_001378493.1:c.-93-251del NP_001365422.1:n.-93-251del