Canonical Allele Identifier: CA117865
Gene: CLDN16 HGNC NCBI

Linked Data

ClinVar Variation Id: 5932
ClinVar RCV Id: RCV000006295
dbSNP Id: rs104893727

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408419G>A , CM000665.2:g.190408419G>A GRCh38
NC_000003.11:g.190126208G>A , CM000665.1:g.190126208G>A GRCh37
NC_000003.10:g.191608902G>A NCBI36
NG_008149.1:g.25368G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.488G>A MANE Select ENSP00000264734.3:p.Gly163Asp
ENST00000456423.2:c.115-1484G>A ENSP00000414136.2:n.115-1484G>A
ENST00000264734.2:c.698G>A ENSP00000264734.2:p.Gly233Asp
ENST00000456423.1:c.325-1484G>A ENSP00000414136.1:n.325-1484G>A
NM_006580.3:c.698G>A NP_006571.1:p.Gly233Asp
NM_001378492.1:c.488G>A NP_001365421.1:p.Gly163Asp
NM_001378493.1:c.488G>A NP_001365422.1:p.Gly163Asp
NM_006580.4:c.488G>A MANE Select NP_006571.2:p.Gly163Asp