Canonical Allele Identifier: CA355762142

Gene: CLDN16

Linked Data

• MyVariant Identifiers: chr3:g.190105931T>G (hg19) ; chr3:g.190388142T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388142T>G , CM000665.2:g.190388142T>G	GRCh38
NC_000003.11:g.190105931T>G , CM000665.1:g.190105931T>G	GRCh37
NC_000003.10:g.191588625T>G	NCBI36
NG_008149.1:g.5091T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456423.2:c.-188T>G	ENSP00000414136.2:n.-188T>G
ENST00000264734.2:c.23T>G	ENSP00000264734.2:p.Leu8Trp
ENST00000456423.1:c.23T>G	ENSP00000414136.1:p.Leu8Trp
ENST00000468220.1:n.306+13539T>G
NM_006580.3:c.23T>G	NP_006571.1:p.Leu8Trp
NM_001378492.1:c.-93-95T>G	NP_001365421.1:n.-93-95T>G
NM_001378493.1:c.-93-95T>G	NP_001365422.1:n.-93-95T>G