Canonical Allele Identifier: CA89760895

Gene: CLDN16

Linked Data

• dbSNP Id: rs1055827835
• gnomAD v3: 3-190402107-C-A
• gnomAD v4: 3-190402107-C-A
• MyVariant Identifiers: chr3:g.190119896C>A (hg19) ; chr3:g.190402107C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402107C>A , CM000665.2:g.190402107C>A	GRCh38
NC_000003.11:g.190119896C>A , CM000665.1:g.190119896C>A	GRCh37
NC_000003.10:g.191602590C>A	NCBI36
NG_008149.1:g.19056C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.115-230C>A MANE Select	ENSP00000264734.3:n.115-230C>A
ENST00000456423.2:c.115-7796C>A	ENSP00000414136.2:n.115-7796C>A
ENST00000264734.2:c.325-230C>A	ENSP00000264734.2:n.325-230C>A
ENST00000456423.1:c.325-7796C>A	ENSP00000414136.1:n.325-7796C>A
ENST00000468220.1:n.307-230C>A
NM_006580.3:c.325-230C>A	NP_006571.1:n.325-230C>A
NM_001378492.1:c.115-230C>A	NP_001365421.1:n.115-230C>A
NM_001378493.1:c.115-230C>A	NP_001365422.1:n.115-230C>A
NM_006580.4:c.115-230C>A MANE Select	NP_006571.2:n.115-230C>A