Canonical Allele Identifier: CA904291014
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs1477816780

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408278T>A , CM000665.2:g.190408278T>A GRCh38
NC_000003.11:g.190126067T>A , CM000665.1:g.190126067T>A GRCh37
NC_000003.10:g.191608761T>A NCBI36
NG_008149.1:g.25227T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.383-36T>A MANE Select ENSP00000264734.3:n.383-36T>A
ENST00000456423.2:c.115-1625T>A ENSP00000414136.2:n.115-1625T>A
ENST00000264734.2:c.593-36T>A ENSP00000264734.2:n.593-36T>A
ENST00000456423.1:c.325-1625T>A ENSP00000414136.1:n.325-1625T>A
NM_006580.3:c.593-36T>A NP_006571.1:n.593-36T>A
NM_001378492.1:c.383-36T>A NP_001365421.1:n.383-36T>A
NM_001378493.1:c.383-36T>A NP_001365422.1:n.383-36T>A
NM_006580.4:c.383-36T>A MANE Select NP_006571.2:n.383-36T>A