Canonical Allele Identifier: CA2830782640

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402387del , CM000665.2:g.190402387del	GRCh38
NC_000003.11:g.190120176del , CM000665.1:g.190120176del	GRCh37
NC_000003.10:g.191602870del	NCBI36
NG_008149.1:g.19336del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.165del MANE Select	ENSP00000264734.3:p.Phe55LeufsTer19
ENST00000456423.2:c.115-7516del	ENSP00000414136.2:n.115-7516del
ENST00000264734.2:c.375del	ENSP00000264734.2:p.Phe125LeufsTer19
ENST00000456423.1:c.325-7516del	ENSP00000414136.1:n.325-7516del
ENST00000468220.1:n.357del
NM_006580.3:c.375del	NP_006571.1:p.Phe125LeufsTer19
NM_001378492.1:c.165del	NP_001365421.1:p.Phe55LeufsTer19
NM_001378493.1:c.165del	NP_001365422.1:p.Phe55LeufsTer19
NM_006580.4:c.165del MANE Select	NP_006571.2:p.Phe55LeufsTer19