Canonical Allele Identifier: CA2669054092
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388031dup , CM000665.2:g.190388031dup GRCh38
NC_000003.11:g.190105820dup , CM000665.1:g.190105820dup GRCh37
NC_000003.10:g.191588514dup NCBI36
NG_008149.1:g.4980dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-89dup ENSP00000264734.2:n.-89dup
ENST00000468220.1:n.306+13428dup
NM_006580.3:c.-89dup NP_006571.1:n.-89dup
NM_001378492.1:c.-93-206dup NP_001365421.1:n.-93-206dup
NM_001378493.1:c.-93-206dup NP_001365422.1:n.-93-206dup