Canonical Allele Identifier: CA1428775572

Gene: CLDN16

Linked Data

• dbSNP Id: rs1718551201

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388122dup , CM000665.2:g.190388122dup	GRCh38
NC_000003.11:g.190105911dup , CM000665.1:g.190105911dup	GRCh37
NC_000003.10:g.191588605dup	NCBI36
NG_008149.1:g.5071dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456423.2:c.-208dup	ENSP00000414136.2:n.-208dup
ENST00000264734.2:c.3dup	ENSP00000264734.2:p.Thr2AspfsTer30
ENST00000456423.1:c.3dup	ENSP00000414136.1:p.Thr2AspfsTer30
ENST00000468220.1:n.306+13519dup
NM_006580.3:c.3dup	NP_006571.1:p.Thr2AspfsTer30
NM_001378492.1:c.-93-115dup	NP_001365421.1:n.-93-115dup
NM_001378493.1:c.-93-115dup	NP_001365422.1:n.-93-115dup