Canonical Allele Identifier: CA355766916
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408316A>G , CM000665.2:g.190408316A>G GRCh38
NC_000003.11:g.190126105A>G , CM000665.1:g.190126105A>G GRCh37
NC_000003.10:g.191608799A>G NCBI36
NG_008149.1:g.25265A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.385A>G MANE Select ENSP00000264734.3:p.Thr129Ala
ENST00000456423.2:c.115-1587A>G ENSP00000414136.2:n.115-1587A>G
ENST00000264734.2:c.595A>G ENSP00000264734.2:p.Thr199Ala
ENST00000456423.1:c.325-1587A>G ENSP00000414136.1:n.325-1587A>G
NM_006580.3:c.595A>G NP_006571.1:p.Thr199Ala
NM_001378492.1:c.385A>G NP_001365421.1:p.Thr129Ala
NM_001378493.1:c.385A>G NP_001365422.1:p.Thr129Ala
NM_006580.4:c.385A>G MANE Select NP_006571.2:p.Thr129Ala