Canonical Allele Identifier: CA355765413
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190402344C>A , CM000665.2:g.190402344C>A GRCh38
NC_000003.11:g.190120133C>A , CM000665.1:g.190120133C>A GRCh37
NC_000003.10:g.191602827C>A NCBI36
NG_008149.1:g.19293C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.122C>A MANE Select ENSP00000264734.3:p.Thr41Lys
ENST00000456423.2:c.115-7559C>A ENSP00000414136.2:n.115-7559C>A
ENST00000264734.2:c.332C>A ENSP00000264734.2:p.Thr111Lys
ENST00000456423.1:c.325-7559C>A ENSP00000414136.1:n.325-7559C>A
ENST00000468220.1:n.314C>A
NM_006580.3:c.332C>A NP_006571.1:p.Thr111Lys
NM_001378492.1:c.122C>A NP_001365421.1:p.Thr41Lys
NM_001378493.1:c.122C>A NP_001365422.1:p.Thr41Lys
NM_006580.4:c.122C>A MANE Select NP_006571.2:p.Thr41Lys