Canonical Allele Identifier: CA355452090

Gene: CLCN2 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.184073194A>T (hg19) ; chr3:g.184355406A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184355406A>T , CM000665.2:g.184355406A>T	GRCh38
NC_000003.11:g.184073194A>T , CM000665.1:g.184073194A>T	GRCh37
NC_000003.10:g.185555888A>T	NCBI36
NG_016422.1:g.11198T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265593.9:c.1294T>A (CLCN2) MANE Select	ENSP00000265593.4:p.Phe432Ile
ENST00000475279.2:c.676T>A (CLCN2)
ENST00000636180.1:c.*270T>A (CLCN2)	ENSP00000490374.1:n.*270T>A
ENST00000636241.1:c.1185T>A (CLCN2)
ENST00000636492.1:c.1177T>A (CLCN2)	ENSP00000490313.1:p.Phe393Ile
ENST00000636658.1:c.555T>A (CLCN2)
ENST00000636661.1:c.*1484T>A (CLCN2)	ENSP00000490764.1:n.*1484T>A
ENST00000637392.1:n.2570T>A (CLCN2)
ENST00000637538.1:c.600T>A (CLCN2)
ENST00000637909.1:c.1100T>A (CLCN2)
ENST00000638134.1:c.1102T>A (CLCN2)
ENST00000265593.8:c.1294T>A (CLCN2)	ENSP00000265593.4:p.Phe432Ile
ENST00000344937.11:c.1294T>A (CLCN2)	ENSP00000345056.7:p.Phe432Ile
ENST00000430397.5:c.237T>A (CLCN2)
ENST00000434054.6:c.1162T>A (CLCN2)	ENSP00000400425.2:p.Phe388Ile
ENST00000444495.1:c.2106+210699A>T (EIF2B5)	ENSP00000409142.1:n.2106+210699A>T
ENST00000457512.1:c.1294T>A (CLCN2)	ENSP00000391928.1:p.Phe432Ile
ENST00000475279.1:n.312T>A (CLCN2)
ENST00000485667.1:n.1301T>A (CLCN2)
NM_001171087.2:c.1294T>A (CLCN2)	NP_001164558.1:p.Phe432Ile
NM_001171088.2:c.1162T>A (CLCN2)	NP_001164559.1:p.Phe388Ile
NM_001171089.2:c.1294T>A (CLCN2)	NP_001164560.1:p.Phe432Ile
NM_004366.5:c.1294T>A (CLCN2)	NP_004357.3:p.Phe432Ile
XM_006713489.1:c.1294T>A (CLCN2)	XP_006713552.1:p.Phe432Ile
XM_006713490.1:c.136T>A (CLCN2)	XP_006713553.1:p.Phe46Ile
XM_011512401.1:c.1294T>A (CLCN2)	XP_011510703.1:p.Phe432Ile
XM_011512402.1:c.1294T>A (CLCN2)	XP_011510704.1:p.Phe432Ile
XM_006713490.2:c.136T>A (CLCN2)	XP_006713553.1:p.Phe46Ile
XR_001740001.1:n.1418T>A (CLCN2)
XR_001740002.1:n.1418T>A (CLCN2)
NM_004366.6:c.1294T>A (CLCN2) MANE Select	NP_004357.3:p.Phe432Ile
NM_001171087.3:c.1294T>A (CLCN2)	NP_001164558.1:p.Phe432Ile
NM_001171088.3:c.1162T>A (CLCN2)	NP_001164559.1:p.Phe388Ile
NM_001171089.3:c.1294T>A (CLCN2)	NP_001164560.1:p.Phe432Ile