Canonical Allele Identifier: CA1428775458
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388032C= , CM000665.2:g.190388032C= GRCh38
NC_000003.11:g.190105821C= , CM000665.1:g.190105821C= GRCh37
NC_000003.10:g.191588515C= NCBI36
NG_008149.1:g.4981C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-88C= ENSP00000264734.2:n.-88C=
ENST00000468220.1:n.306+13429C=
NM_006580.3:c.-88C= NP_006571.1:n.-88C=
NM_001378492.1:c.-93-205C= NP_001365421.1:n.-93-205C=
NM_001378493.1:c.-93-205C= NP_001365422.1:n.-93-205C=