Canonical Allele Identifier: CA437167620

Gene: CLCN2 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.184073533G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184355745G>C , CM000665.2:g.184355745G>C	GRCh38
NC_000003.11:g.184073533G>C , CM000665.1:g.184073533G>C	GRCh37
NC_000003.10:g.185556227G>C	NCBI36
NG_016422.1:g.10859C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265593.9:c.1119C>G (CLCN2) MANE Select	ENSP00000265593.4:p.Leu373=
ENST00000475279.2:c.501C>G (CLCN2)
ENST00000636180.1:c.*95C>G (CLCN2)	ENSP00000490374.1:n.*95C>G
ENST00000636241.1:c.1010C>G (CLCN2)
ENST00000636492.1:c.1002C>G (CLCN2)	ENSP00000490313.1:p.Leu334=
ENST00000636658.1:c.380C>G (CLCN2)
ENST00000636661.1:c.*1309C>G (CLCN2)	ENSP00000490764.1:n.*1309C>G
ENST00000637392.1:n.2231C>G (CLCN2)
ENST00000637538.1:c.425C>G (CLCN2)
ENST00000637909.1:c.925C>G (CLCN2)
ENST00000638134.1:c.927C>G (CLCN2)
ENST00000265593.8:c.1119C>G (CLCN2)	ENSP00000265593.4:p.Leu373=
ENST00000344937.11:c.1119C>G (CLCN2)	ENSP00000345056.7:p.Leu373=
ENST00000430397.5:c.62C>G (CLCN2)
ENST00000434054.6:c.987C>G (CLCN2)	ENSP00000400425.2:p.Leu329=
ENST00000444495.1:c.2106+211038G>C (EIF2B5)	ENSP00000409142.1:n.2106+211038G>C
ENST00000457512.1:c.1119C>G (CLCN2)	ENSP00000391928.1:p.Leu373=
ENST00000475279.1:n.137C>G (CLCN2)
ENST00000485667.1:n.1126C>G (CLCN2)
NM_001171087.2:c.1119C>G (CLCN2)	NP_001164558.1:p.Leu373=
NM_001171088.2:c.987C>G (CLCN2)	NP_001164559.1:p.Leu329=
NM_001171089.2:c.1119C>G (CLCN2)	NP_001164560.1:p.Leu373=
NM_004366.5:c.1119C>G (CLCN2)	NP_004357.3:p.Leu373=
XM_006713489.1:c.1119C>G (CLCN2)	XP_006713552.1:p.Leu373=
XM_006713490.1:c.-40C>G (CLCN2)	XP_006713553.1:n.-40C>G
XM_011512401.1:c.1119C>G (CLCN2)	XP_011510703.1:p.Leu373=
XM_011512402.1:c.1119C>G (CLCN2)	XP_011510704.1:p.Leu373=
XM_006713490.2:c.-40C>G (CLCN2)	XP_006713553.1:n.-40C>G
XR_001740001.1:n.1243C>G (CLCN2)
XR_001740002.1:n.1243C>G (CLCN2)
NM_004366.6:c.1119C>G (CLCN2) MANE Select	NP_004357.3:p.Leu373=
NM_001171087.3:c.1119C>G (CLCN2)	NP_001164558.1:p.Leu373=
NM_001171088.3:c.987C>G (CLCN2)	NP_001164559.1:p.Leu329=
NM_001171089.3:c.1119C>G (CLCN2)	NP_001164560.1:p.Leu373=