Canonical Allele Identifier: CA2669041334

Gene: CLDN16

Linked Data

• gnomAD v4: 3-190402516-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402518_190402519del , CM000665.2:g.190402518_190402519del	GRCh38
NC_000003.11:g.190120307_190120308del , CM000665.1:g.190120307_190120308del	GRCh37
NC_000003.10:g.191603001_191603002del	NCBI36
NG_008149.1:g.19467_19468del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.217+79_217+80del MANE Select	ENSP00000264734.3:n.217+79_217+80del
ENST00000456423.2:c.115-7385_115-7384del	ENSP00000414136.2:n.115-7385_115-7384del
ENST00000264734.2:c.427+79_427+80del	ENSP00000264734.2:n.427+79_427+80del
ENST00000456423.1:c.325-7385_325-7384del	ENSP00000414136.1:n.325-7385_325-7384del
ENST00000468220.1:n.409+79_409+80del
NM_006580.3:c.427+79_427+80del	NP_006571.1:n.427+79_427+80del
NM_001378492.1:c.217+79_217+80del	NP_001365421.1:n.217+79_217+80del
NM_001378493.1:c.217+79_217+80del	NP_001365422.1:n.217+79_217+80del
NM_006580.4:c.217+79_217+80del MANE Select	NP_006571.2:n.217+79_217+80del