Canonical Allele Identifier: CA2669054103
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388055del , CM000665.2:g.190388055del GRCh38
NC_000003.11:g.190105844del , CM000665.1:g.190105844del GRCh37
NC_000003.10:g.191588538del NCBI36
NG_008149.1:g.5004del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-65del ENSP00000264734.2:n.-65del
ENST00000468220.1:n.306+13452del
NM_006580.3:c.-65del NP_006571.1:n.-65del
NM_001378492.1:c.-93-182del NP_001365421.1:n.-93-182del
NM_001378493.1:c.-93-182del NP_001365422.1:n.-93-182del