Canonical Allele Identifier: CA1428775448
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388018G= , CM000665.2:g.190388018G= GRCh38
NC_000003.11:g.190105807G= , CM000665.1:g.190105807G= GRCh37
NC_000003.10:g.191588501G= NCBI36
NG_008149.1:g.4967G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-102G= ENSP00000264734.2:n.-102G=
ENST00000468220.1:n.306+13415G=
NM_006580.3:c.-102G= NP_006571.1:n.-102G=
NM_001378492.1:c.-93-219G= NP_001365421.1:n.-93-219G=
NM_001378493.1:c.-93-219G= NP_001365422.1:n.-93-219G=