Canonical Allele Identifier: CA355765818

Gene: CLDN16

Linked Data

• MyVariant Identifiers: chr3:g.190120222C>G (hg19) ; chr3:g.190402433C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402433C>G , CM000665.2:g.190402433C>G	GRCh38
NC_000003.11:g.190120222C>G , CM000665.1:g.190120222C>G	GRCh37
NC_000003.10:g.191602916C>G	NCBI36
NG_008149.1:g.19382C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264734.3:c.211C>G MANE Select	ENSP00000264734.3:p.His71Asp
ENST00000456423.2:c.115-7470C>G	ENSP00000414136.2:n.115-7470C>G
ENST00000264734.2:c.421C>G	ENSP00000264734.2:p.His141Asp
ENST00000456423.1:c.325-7470C>G	ENSP00000414136.1:n.325-7470C>G
ENST00000468220.1:n.403C>G
NM_006580.3:c.421C>G	NP_006571.1:p.His141Asp
NM_001378492.1:c.211C>G	NP_001365421.1:p.His71Asp
NM_001378493.1:c.211C>G	NP_001365422.1:p.His71Asp
NM_006580.4:c.211C>G MANE Select	NP_006571.2:p.His71Asp