Canonical Allele Identifier: CA355451937

Gene: CLCN2 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.184073175A>C (hg19) ; chr3:g.184355387A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184355387A>C , CM000665.2:g.184355387A>C	GRCh38
NC_000003.11:g.184073175A>C , CM000665.1:g.184073175A>C	GRCh37
NC_000003.10:g.185555869A>C	NCBI36
NG_016422.1:g.11217T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265593.9:c.1313T>G (CLCN2) MANE Select	ENSP00000265593.4:p.Phe438Cys
ENST00000475279.2:c.695T>G (CLCN2)
ENST00000636180.1:c.*289T>G (CLCN2)	ENSP00000490374.1:n.*289T>G
ENST00000636241.1:c.1204T>G (CLCN2)
ENST00000636492.1:c.1196T>G (CLCN2)	ENSP00000490313.1:p.Phe399Cys
ENST00000636658.1:c.574T>G (CLCN2)
ENST00000636661.1:c.*1503T>G (CLCN2)	ENSP00000490764.1:n.*1503T>G
ENST00000637392.1:n.2589T>G (CLCN2)
ENST00000637538.1:c.619T>G (CLCN2)
ENST00000637909.1:c.1119T>G (CLCN2)
ENST00000638134.1:c.1121T>G (CLCN2)
ENST00000265593.8:c.1313T>G (CLCN2)	ENSP00000265593.4:p.Phe438Cys
ENST00000344937.11:c.1313T>G (CLCN2)	ENSP00000345056.7:p.Phe438Cys
ENST00000430397.5:c.256T>G (CLCN2)
ENST00000434054.6:c.1181T>G (CLCN2)	ENSP00000400425.2:p.Phe394Cys
ENST00000444495.1:c.2106+210680A>C (EIF2B5)	ENSP00000409142.1:n.2106+210680A>C
ENST00000457512.1:c.1313T>G (CLCN2)	ENSP00000391928.1:p.Phe438Cys
ENST00000485667.1:n.1320T>G (CLCN2)
NM_001171087.2:c.1313T>G (CLCN2)	NP_001164558.1:p.Phe438Cys
NM_001171088.2:c.1181T>G (CLCN2)	NP_001164559.1:p.Phe394Cys
NM_001171089.2:c.1313T>G (CLCN2)	NP_001164560.1:p.Phe438Cys
NM_004366.5:c.1313T>G (CLCN2)	NP_004357.3:p.Phe438Cys
XM_006713489.1:c.1313T>G (CLCN2)	XP_006713552.1:p.Phe438Cys
XM_006713490.1:c.155T>G (CLCN2)	XP_006713553.1:p.Phe52Cys
XM_011512401.1:c.1313T>G (CLCN2)	XP_011510703.1:p.Phe438Cys
XM_011512402.1:c.1313T>G (CLCN2)	XP_011510704.1:p.Phe438Cys
XM_006713490.2:c.155T>G (CLCN2)	XP_006713553.1:p.Phe52Cys
XR_001740001.1:n.1437T>G (CLCN2)
XR_001740002.1:n.1437T>G (CLCN2)
NM_004366.6:c.1313T>G (CLCN2) MANE Select	NP_004357.3:p.Phe438Cys
NM_001171087.3:c.1313T>G (CLCN2)	NP_001164558.1:p.Phe438Cys
NM_001171088.3:c.1181T>G (CLCN2)	NP_001164559.1:p.Phe394Cys
NM_001171089.3:c.1313T>G (CLCN2)	NP_001164560.1:p.Phe438Cys