Canonical Allele Identifier: CA355767172
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408432G>T , CM000665.2:g.190408432G>T GRCh38
NC_000003.11:g.190126221G>T , CM000665.1:g.190126221G>T GRCh37
NC_000003.10:g.191608915G>T NCBI36
NG_008149.1:g.25381G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.501G>T MANE Select ENSP00000264734.3:p.Trp167Cys
ENST00000456423.2:c.115-1471G>T ENSP00000414136.2:n.115-1471G>T
ENST00000264734.2:c.711G>T ENSP00000264734.2:p.Trp237Cys
ENST00000456423.1:c.325-1471G>T ENSP00000414136.1:n.325-1471G>T
NM_006580.3:c.711G>T NP_006571.1:p.Trp237Cys
NM_001378492.1:c.501G>T NP_001365421.1:p.Trp167Cys
NM_001378493.1:c.501G>T NP_001365422.1:p.Trp167Cys
NM_006580.4:c.501G>T MANE Select NP_006571.2:p.Trp167Cys