Canonical Allele Identifier: CA1428759252

Gene: CLDN16

Linked Data

• ClinVar Variation Id: 1028524
• ClinVar RCV Id: RCV001329585
• dbSNP Id: rs1719047633

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190404752G>A , CM000665.2:g.190404752G>A	GRCh38
NC_000003.11:g.190122541G>A , CM000665.1:g.190122541G>A	GRCh37
NC_000003.10:g.191605235G>A	NCBI36
NG_008149.1:g.21701G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.218-10G>A MANE Select	ENSP00000264734.3:n.218-10G>A
ENST00000456423.2:c.115-5151G>A	ENSP00000414136.2:n.115-5151G>A
ENST00000264734.2:c.428-10G>A	ENSP00000264734.2:n.428-10G>A
ENST00000456423.1:c.325-5151G>A	ENSP00000414136.1:n.325-5151G>A
ENST00000468220.1:n.410-10G>A
NM_006580.3:c.428-10G>A	NP_006571.1:n.428-10G>A
NM_001378492.1:c.218-10G>A	NP_001365421.1:n.218-10G>A
NM_001378493.1:c.218-10G>A	NP_001365422.1:n.218-10G>A
NM_006580.4:c.218-10G>A MANE Select	NP_006571.2:n.218-10G>A