Canonical Allele Identifier: CA437418490

Gene: CLDN16

Linked Data

• MyVariant Identifiers: chr3:g.190122681C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190404892C>A , CM000665.2:g.190404892C>A	GRCh38
NC_000003.11:g.190122681C>A , CM000665.1:g.190122681C>A	GRCh37
NC_000003.10:g.191605375C>A	NCBI36
NG_008149.1:g.21841C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.348C>A MANE Select	ENSP00000264734.3:p.Ile116=
ENST00000456423.2:c.115-5011C>A	ENSP00000414136.2:n.115-5011C>A
ENST00000264734.2:c.558C>A	ENSP00000264734.2:p.Ile186=
ENST00000456423.1:c.325-5011C>A	ENSP00000414136.1:n.325-5011C>A
ENST00000468220.1:n.540C>A
NM_006580.3:c.558C>A	NP_006571.1:p.Ile186=
NM_001378492.1:c.348C>A	NP_001365421.1:p.Ile116=
NM_001378493.1:c.348C>A	NP_001365422.1:p.Ile116=
NM_006580.4:c.348C>A MANE Select	NP_006571.2:p.Ile116=