Canonical Allele Identifier: CA1057666511

Gene: CLDN16

Linked Data

• dbSNP Id: rs1718980574
• gnomAD v3: 3-190402227-T-TAACC
• gnomAD v4: 3-190402227-T-TAACC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402229_190402232dup , CM000665.2:g.190402229_190402232dup	GRCh38
NC_000003.11:g.190120018_190120021dup , CM000665.1:g.190120018_190120021dup	GRCh37
NC_000003.10:g.191602712_191602715dup	NCBI36
NG_008149.1:g.19178_19181dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.115-108_115-105dup MANE Select	ENSP00000264734.3:n.115-108_115-105dup
ENST00000456423.2:c.115-7674_115-7671dup	ENSP00000414136.2:n.115-7674_115-7671dup
ENST00000264734.2:c.325-108_325-105dup	ENSP00000264734.2:n.325-108_325-105dup
ENST00000456423.1:c.325-7674_325-7671dup	ENSP00000414136.1:n.325-7674_325-7671dup
ENST00000468220.1:n.307-108_307-105dup
NM_006580.3:c.325-108_325-105dup	NP_006571.1:n.325-108_325-105dup
NM_001378492.1:c.115-108_115-105dup	NP_001365421.1:n.115-108_115-105dup
NM_001378493.1:c.115-108_115-105dup	NP_001365422.1:n.115-108_115-105dup
NM_006580.4:c.115-108_115-105dup MANE Select	NP_006571.2:n.115-108_115-105dup