Canonical Allele Identifier: CA1428775951

Gene: CLDN16

Linked Data

• dbSNP Id: rs1718561243

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388332dup , CM000665.2:g.190388332dup	GRCh38
NC_000003.11:g.190106121dup , CM000665.1:g.190106121dup	GRCh37
NC_000003.10:g.191588815dup	NCBI36
NG_008149.1:g.5281dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000264734.3:c.3dup MANE Select	ENSP00000264734.3:p.Arg2GlufsTer26
ENST00000456423.2:c.3dup	ENSP00000414136.2:p.Arg2GlufsTer26
ENST00000264734.2:c.213dup	ENSP00000264734.2:p.Arg72GlufsTer26
ENST00000456423.1:c.213dup	ENSP00000414136.1:p.Arg72GlufsTer26
ENST00000468220.1:n.306+13729dup
NM_006580.3:c.213dup	NP_006571.1:p.Arg72GlufsTer26
NM_001378492.1:c.3dup	NP_001365421.1:p.Arg2GlufsTer26
NM_001378493.1:c.3dup	NP_001365422.1:p.Arg2GlufsTer26
NM_006580.4:c.3dup MANE Select	NP_006571.2:p.Arg2GlufsTer26