Canonical Allele Identifier: CA2753863
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs762220084

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408333C>T , CM000665.2:g.190408333C>T GRCh38
NC_000003.11:g.190126122C>T , CM000665.1:g.190126122C>T GRCh37
NC_000003.10:g.191608816C>T NCBI36
NG_008149.1:g.25282C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.402C>T MANE Select ENSP00000264734.3:p.Gly134=
ENST00000456423.2:c.115-1570C>T ENSP00000414136.2:n.115-1570C>T
ENST00000264734.2:c.612C>T ENSP00000264734.2:p.Gly204=
ENST00000456423.1:c.325-1570C>T ENSP00000414136.1:n.325-1570C>T
NM_006580.3:c.612C>T NP_006571.1:p.Gly204=
NM_001378492.1:c.402C>T NP_001365421.1:p.Gly134=
NM_001378493.1:c.402C>T NP_001365422.1:p.Gly134=
NM_006580.4:c.402C>T MANE Select NP_006571.2:p.Gly134=