Canonical Allele Identifier: CA89763199

Gene: CLDN16

Linked Data

• dbSNP Id: rs926293551
• MyVariant Identifiers: chr3:g.190122540T>A (hg19) ; chr3:g.190404751T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190404751T>A , CM000665.2:g.190404751T>A	GRCh38
NC_000003.11:g.190122540T>A , CM000665.1:g.190122540T>A	GRCh37
NC_000003.10:g.191605234T>A	NCBI36
NG_008149.1:g.21700T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.218-11T>A MANE Select	ENSP00000264734.3:n.218-11T>A
ENST00000456423.2:c.115-5152T>A	ENSP00000414136.2:n.115-5152T>A
ENST00000264734.2:c.428-11T>A	ENSP00000264734.2:n.428-11T>A
ENST00000456423.1:c.325-5152T>A	ENSP00000414136.1:n.325-5152T>A
ENST00000468220.1:n.410-11T>A
NM_006580.3:c.428-11T>A	NP_006571.1:n.428-11T>A
NM_001378492.1:c.218-11T>A	NP_001365421.1:n.218-11T>A
NM_001378493.1:c.218-11T>A	NP_001365422.1:n.218-11T>A
NM_006580.4:c.218-11T>A MANE Select	NP_006571.2:n.218-11T>A