Canonical Allele Identifier: CA1428756701

Gene: CLDN16

Linked Data

• dbSNP Id: rs1701230767

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402144C>G , CM000665.2:g.190402144C>G	GRCh38
NC_000003.11:g.190119933C>G , CM000665.1:g.190119933C>G	GRCh37
NC_000003.10:g.191602627C>G	NCBI36
NG_008149.1:g.19093C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.115-193C>G MANE Select	ENSP00000264734.3:n.115-193C>G
ENST00000456423.2:c.115-7759C>G	ENSP00000414136.2:n.115-7759C>G
ENST00000264734.2:c.325-193C>G	ENSP00000264734.2:n.325-193C>G
ENST00000456423.1:c.325-7759C>G	ENSP00000414136.1:n.325-7759C>G
ENST00000468220.1:n.307-193C>G
NM_006580.3:c.325-193C>G	NP_006571.1:n.325-193C>G
NM_001378492.1:c.115-193C>G	NP_001365421.1:n.115-193C>G
NM_001378493.1:c.115-193C>G	NP_001365422.1:n.115-193C>G
NM_006580.4:c.115-193C>G MANE Select	NP_006571.2:n.115-193C>G