Canonical Allele Identifier: CA355765581
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190402381T>A , CM000665.2:g.190402381T>A GRCh38
NC_000003.11:g.190120170T>A , CM000665.1:g.190120170T>A GRCh37
NC_000003.10:g.191602864T>A NCBI36
NG_008149.1:g.19330T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.159T>A MANE Select ENSP00000264734.3:p.Asn53Lys
ENST00000456423.2:c.115-7522T>A ENSP00000414136.2:n.115-7522T>A
ENST00000264734.2:c.369T>A ENSP00000264734.2:p.Asn123Lys
ENST00000456423.1:c.325-7522T>A ENSP00000414136.1:n.325-7522T>A
ENST00000468220.1:n.351T>A
NM_006580.3:c.369T>A NP_006571.1:p.Asn123Lys
NM_001378492.1:c.159T>A NP_001365421.1:p.Asn53Lys
NM_001378493.1:c.159T>A NP_001365422.1:p.Asn53Lys
NM_006580.4:c.159T>A MANE Select NP_006571.2:p.Asn53Lys