Canonical Allele Identifier: CA355762137
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388139T>C , CM000665.2:g.190388139T>C GRCh38
NC_000003.11:g.190105928T>C , CM000665.1:g.190105928T>C GRCh37
NC_000003.10:g.191588622T>C NCBI36
NG_008149.1:g.5088T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000456423.2:c.-191T>C ENSP00000414136.2:n.-191T>C
ENST00000264734.2:c.20T>C ENSP00000264734.2:p.Leu7Pro
ENST00000456423.1:c.20T>C ENSP00000414136.1:p.Leu7Pro
ENST00000468220.1:n.306+13536T>C
NM_006580.3:c.20T>C NP_006571.1:p.Leu7Pro
NM_001378492.1:c.-93-98T>C NP_001365421.1:n.-93-98T>C
NM_001378493.1:c.-93-98T>C NP_001365422.1:n.-93-98T>C