Canonical Allele Identifier: CA1428757200

Gene: CLDN16

Linked Data

• dbSNP Id: rs1718990144

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402517_190402518insCACC , CM000665.2:g.190402517_190402518insCACC	GRCh38
NC_000003.11:g.190120306_190120307insCACC , CM000665.1:g.190120306_190120307insCACC	GRCh37
NC_000003.10:g.191603000_191603001insCACC	NCBI36
NG_008149.1:g.19466_19467insCACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.217+78_217+79insCACC MANE Select	ENSP00000264734.3:n.217+78_217+79insCACC
ENST00000456423.2:c.115-7386_115-7385insCACC	ENSP00000414136.2:n.115-7386_115-7385insCACC
ENST00000264734.2:c.427+78_427+79insCACC	ENSP00000264734.2:n.427+78_427+79insCACC
ENST00000456423.1:c.325-7386_325-7385insCACC	ENSP00000414136.1:n.325-7386_325-7385insCACC
ENST00000468220.1:n.409+78_409+79insCACC
NM_006580.3:c.427+78_427+79insCACC	NP_006571.1:n.427+78_427+79insCACC
NM_001378492.1:c.217+78_217+79insCACC	NP_001365421.1:n.217+78_217+79insCACC
NM_001378493.1:c.217+78_217+79insCACC	NP_001365422.1:n.217+78_217+79insCACC
NM_006580.4:c.217+78_217+79insCACC MANE Select	NP_006571.2:n.217+78_217+79insCACC