Canonical Allele Identifier: CA117870
Gene: CLDN16 HGNC NCBI

Linked Data

ClinVar Variation Id: 5937
ClinVar RCV Id: RCV000006300
dbSNP Id: rs104893732

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190402362G>A , CM000665.2:g.190402362G>A GRCh38
NC_000003.11:g.190120151G>A , CM000665.1:g.190120151G>A GRCh37
NC_000003.10:g.191602845G>A NCBI36
NG_008149.1:g.19311G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.140G>A MANE Select ENSP00000264734.3:p.Trp47Ter
ENST00000456423.2:c.115-7541G>A ENSP00000414136.2:n.115-7541G>A
ENST00000264734.2:c.350G>A ENSP00000264734.2:p.Trp117Ter
ENST00000456423.1:c.325-7541G>A ENSP00000414136.1:n.325-7541G>A
ENST00000468220.1:n.332G>A
NM_006580.3:c.350G>A NP_006571.1:p.Trp117Ter
NM_001378492.1:c.140G>A NP_001365421.1:p.Trp47Ter
NM_001378493.1:c.140G>A NP_001365422.1:p.Trp47Ter
NM_006580.4:c.140G>A MANE Select NP_006571.2:p.Trp47Ter