Canonical Allele Identifier: CA1425984306

Gene: CLCN2 EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184355399G= , CM000665.2:g.184355399G=	GRCh38
NC_000003.11:g.184073187G= , CM000665.1:g.184073187G=	GRCh37
NC_000003.10:g.185555881G=	NCBI36
NG_016422.1:g.11205C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265593.9:c.1301C= (CLCN2) MANE Select	ENSP00000265593.4:p.Thr434=
ENST00000475279.2:c.683C= (CLCN2)
ENST00000636180.1:c.*277C= (CLCN2)	ENSP00000490374.1:n.*277C=
ENST00000636241.1:c.1192C= (CLCN2)
ENST00000636492.1:c.1184C= (CLCN2)	ENSP00000490313.1:p.Thr395=
ENST00000636658.1:c.562C= (CLCN2)
ENST00000636661.1:c.*1491C= (CLCN2)	ENSP00000490764.1:n.*1491C=
ENST00000637392.1:n.2577C= (CLCN2)
ENST00000637538.1:c.607C= (CLCN2)
ENST00000637909.1:c.1107C= (CLCN2)
ENST00000638134.1:c.1109C= (CLCN2)
ENST00000265593.8:c.1301C= (CLCN2)	ENSP00000265593.4:p.Thr434=
ENST00000344937.11:c.1301C= (CLCN2)	ENSP00000345056.7:p.Thr434=
ENST00000430397.5:c.244C= (CLCN2)
ENST00000434054.6:c.1169C= (CLCN2)	ENSP00000400425.2:p.Thr390=
ENST00000444495.1:c.2106+210692G= (EIF2B5)	ENSP00000409142.1:n.2106+210692G=
ENST00000457512.1:c.1301C= (CLCN2)	ENSP00000391928.1:p.Thr434=
ENST00000485667.1:n.1308C= (CLCN2)
NM_001171087.2:c.1301C= (CLCN2)	NP_001164558.1:p.Thr434=
NM_001171088.2:c.1169C= (CLCN2)	NP_001164559.1:p.Thr390=
NM_001171089.2:c.1301C= (CLCN2)	NP_001164560.1:p.Thr434=
NM_004366.5:c.1301C= (CLCN2)	NP_004357.3:p.Thr434=
XM_006713489.1:c.1301C= (CLCN2)	XP_006713552.1:p.Thr434=
XM_006713490.1:c.143C= (CLCN2)	XP_006713553.1:p.Thr48=
XM_011512401.1:c.1301C= (CLCN2)	XP_011510703.1:p.Thr434=
XM_011512402.1:c.1301C= (CLCN2)	XP_011510704.1:p.Thr434=
XM_006713490.2:c.143C= (CLCN2)	XP_006713553.1:p.Thr48=
XR_001740001.1:n.1425C= (CLCN2)
XR_001740002.1:n.1425C= (CLCN2)
NM_004366.6:c.1301C= (CLCN2) MANE Select	NP_004357.3:p.Thr434=
NM_001171087.3:c.1301C= (CLCN2)	NP_001164558.1:p.Thr434=
NM_001171088.3:c.1169C= (CLCN2)	NP_001164559.1:p.Thr390=
NM_001171089.3:c.1301C= (CLCN2)	NP_001164560.1:p.Thr434=