Canonical Allele Identifier: CA89749982

Gene: CLDN16

Linked Data

• dbSNP Id: rs386669518

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388284_190388285delinsC , CM000665.2:g.190388284_190388285delinsC	GRCh38
NC_000003.11:g.190106073_190106074delinsC , CM000665.1:g.190106073_190106074delinsC	GRCh37
NC_000003.10:g.191588767_191588768delinsC	NCBI36
NG_008149.1:g.5233_5234delinsC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.-46_-45delinsC MANE Select	ENSP00000264734.3:n.-46_-45delinsC
ENST00000456423.2:c.-46_-45delinsC	ENSP00000414136.2:n.-46_-45delinsC
ENST00000264734.2:c.165_166delinsC	ENSP00000264734.2:p.Arg55SerfsTer17
ENST00000456423.1:c.165_166delinsC	ENSP00000414136.1:p.Arg55SerfsTer17
ENST00000468220.1:n.306+13681_306+13682delinsC
NM_006580.3:c.165_166delinsC	NP_006571.1:p.Arg55SerfsTer17
NM_001378492.1:c.-46_-45delinsC	NP_001365421.1:n.-46_-45delinsC
NM_001378493.1:c.-46_-45delinsC	NP_001365422.1:n.-46_-45delinsC
NM_006580.4:c.-46_-45delinsC MANE Select	NP_006571.2:n.-46_-45delinsC