Canonical Allele Identifier: CA117861
Gene: CLDN16 HGNC NCBI

Linked Data

ClinVar Variation Id: 5928
ClinVar RCV Id: RCV000006291
dbSNP Id: rs104893723

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408314G>A , CM000665.2:g.190408314G>A GRCh38
NC_000003.11:g.190126103G>A , CM000665.1:g.190126103G>A GRCh37
NC_000003.10:g.191608797G>A NCBI36
NG_008149.1:g.25263G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.383G>A MANE Select ENSP00000264734.3:p.Gly128Asp
ENST00000456423.2:c.115-1589G>A ENSP00000414136.2:n.115-1589G>A
ENST00000264734.2:c.593G>A ENSP00000264734.2:p.Gly198Asp
ENST00000456423.1:c.325-1589G>A ENSP00000414136.1:n.325-1589G>A
NM_006580.3:c.593G>A NP_006571.1:p.Gly198Asp
NM_001378492.1:c.383G>A NP_001365421.1:p.Gly128Asp
NM_001378493.1:c.383G>A NP_001365422.1:p.Gly128Asp
NM_006580.4:c.383G>A MANE Select NP_006571.2:p.Gly128Asp