Canonical Allele Identifier: CA355765772

Gene: CLDN16

Linked Data

• MyVariant Identifiers: chr3:g.190120211T>G (hg19) ; chr3:g.190402422T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402422T>G , CM000665.2:g.190402422T>G	GRCh38
NC_000003.11:g.190120211T>G , CM000665.1:g.190120211T>G	GRCh37
NC_000003.10:g.191602905T>G	NCBI36
NG_008149.1:g.19371T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.200T>G MANE Select	ENSP00000264734.3:p.Ile67Arg
ENST00000456423.2:c.115-7481T>G	ENSP00000414136.2:n.115-7481T>G
ENST00000264734.2:c.410T>G	ENSP00000264734.2:p.Ile137Arg
ENST00000456423.1:c.325-7481T>G	ENSP00000414136.1:n.325-7481T>G
ENST00000468220.1:n.392T>G
NM_006580.3:c.410T>G	NP_006571.1:p.Ile137Arg
NM_001378492.1:c.200T>G	NP_001365421.1:p.Ile67Arg
NM_001378493.1:c.200T>G	NP_001365422.1:p.Ile67Arg
NM_006580.4:c.200T>G MANE Select	NP_006571.2:p.Ile67Arg