Canonical Allele Identifier: CA355762236
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388184A>T , CM000665.2:g.190388184A>T GRCh38
NC_000003.11:g.190105973A>T , CM000665.1:g.190105973A>T GRCh37
NC_000003.10:g.191588667A>T NCBI36
NG_008149.1:g.5133A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.-146A>T MANE Select ENSP00000264734.3:n.-146A>T
ENST00000456423.2:c.-146A>T ENSP00000414136.2:n.-146A>T
ENST00000264734.2:c.65A>T ENSP00000264734.2:p.His22Leu
ENST00000456423.1:c.65A>T ENSP00000414136.1:p.His22Leu
ENST00000468220.1:n.306+13581A>T
NM_006580.3:c.65A>T NP_006571.1:p.His22Leu
NM_001378492.1:c.-93-53A>T NP_001365421.1:n.-93-53A>T
NM_001378493.1:c.-93-53A>T NP_001365422.1:n.-93-53A>T
NM_006580.4:c.-146A>T MANE Select NP_006571.2:n.-146A>T