Canonical Allele Identifier: CA2840867397

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402493T>G , CM000665.2:g.190402493T>G	GRCh38
NC_000003.11:g.190120282T>G , CM000665.1:g.190120282T>G	GRCh37
NC_000003.10:g.191602976T>G	NCBI36
NG_008149.1:g.19442T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.217+54T>G MANE Select	ENSP00000264734.3:n.217+54T>G
ENST00000456423.2:c.115-7410T>G	ENSP00000414136.2:n.115-7410T>G
ENST00000264734.2:c.427+54T>G	ENSP00000264734.2:n.427+54T>G
ENST00000456423.1:c.325-7410T>G	ENSP00000414136.1:n.325-7410T>G
ENST00000468220.1:n.409+54T>G
NM_006580.3:c.427+54T>G	NP_006571.1:n.427+54T>G
NM_001378492.1:c.217+54T>G	NP_001365421.1:n.217+54T>G
NM_001378493.1:c.217+54T>G	NP_001365422.1:n.217+54T>G
NM_006580.4:c.217+54T>G MANE Select	NP_006571.2:n.217+54T>G