Canonical Allele Identifier: CA355766955
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408334T>G , CM000665.2:g.190408334T>G GRCh38
NC_000003.11:g.190126123T>G , CM000665.1:g.190126123T>G GRCh37
NC_000003.10:g.191608817T>G NCBI36
NG_008149.1:g.25283T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.403T>G MANE Select ENSP00000264734.3:p.Ser135Ala
ENST00000456423.2:c.115-1569T>G ENSP00000414136.2:n.115-1569T>G
ENST00000264734.2:c.613T>G ENSP00000264734.2:p.Ser205Ala
ENST00000456423.1:c.325-1569T>G ENSP00000414136.1:n.325-1569T>G
NM_006580.3:c.613T>G NP_006571.1:p.Ser205Ala
NM_001378492.1:c.403T>G NP_001365421.1:p.Ser135Ala
NM_001378493.1:c.403T>G NP_001365422.1:p.Ser135Ala
NM_006580.4:c.403T>G MANE Select NP_006571.2:p.Ser135Ala