Canonical Allele Identifier: CA355762550
Gene: CLDN16 HGNC NCBI

Linked Data

COSMIC: COSM729983

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388336G>A , CM000665.2:g.190388336G>A GRCh38
NC_000003.11:g.190106125G>A , CM000665.1:g.190106125G>A GRCh37
NC_000003.10:g.191588819G>A NCBI36
NG_008149.1:g.5285G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.7G>A MANE Select ENSP00000264734.3:p.Asp3Asn
ENST00000456423.2:c.7G>A ENSP00000414136.2:p.Asp3Asn
ENST00000264734.2:c.217G>A ENSP00000264734.2:p.Asp73Asn
ENST00000456423.1:c.217G>A ENSP00000414136.1:p.Asp73Asn
ENST00000468220.1:n.306+13733G>A
NM_006580.3:c.217G>A NP_006571.1:p.Asp73Asn
NM_001378492.1:c.7G>A NP_001365421.1:p.Asp3Asn
NM_001378493.1:c.7G>A NP_001365422.1:p.Asp3Asn
NM_006580.4:c.7G>A MANE Select NP_006571.2:p.Asp3Asn