Canonical Allele Identifier: CA355453356

Gene: CLCN2 EIF2B5

Linked Data

• dbSNP Id: rs1728497513
• MyVariant Identifiers: chr3:g.184073489G>T (hg19) ; chr3:g.184355701G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184355701G>T , CM000665.2:g.184355701G>T	GRCh38
NC_000003.11:g.184073489G>T , CM000665.1:g.184073489G>T	GRCh37
NC_000003.10:g.185556183G>T	NCBI36
NG_016422.1:g.10903C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265593.9:c.1163C>A (CLCN2) MANE Select	ENSP00000265593.4:p.Ala388Asp
ENST00000475279.2:c.545C>A (CLCN2)
ENST00000636180.1:c.*139C>A (CLCN2)	ENSP00000490374.1:n.*139C>A
ENST00000636241.1:c.1054C>A (CLCN2)
ENST00000636492.1:c.1046C>A (CLCN2)	ENSP00000490313.1:p.Ala349Asp
ENST00000636658.1:c.424C>A (CLCN2)
ENST00000636661.1:c.*1353C>A (CLCN2)	ENSP00000490764.1:n.*1353C>A
ENST00000637392.1:n.2275C>A (CLCN2)
ENST00000637538.1:c.469C>A (CLCN2)
ENST00000637909.1:c.969C>A (CLCN2)
ENST00000638134.1:c.971C>A (CLCN2)
ENST00000265593.8:c.1163C>A (CLCN2)	ENSP00000265593.4:p.Ala388Asp
ENST00000344937.11:c.1163C>A (CLCN2)	ENSP00000345056.7:p.Ala388Asp
ENST00000430397.5:c.106C>A (CLCN2)
ENST00000434054.6:c.1031C>A (CLCN2)	ENSP00000400425.2:p.Ala344Asp
ENST00000444495.1:c.2106+210994G>T (EIF2B5)	ENSP00000409142.1:n.2106+210994G>T
ENST00000457512.1:c.1163C>A (CLCN2)	ENSP00000391928.1:p.Ala388Asp
ENST00000475279.1:n.181C>A (CLCN2)
ENST00000485667.1:n.1170C>A (CLCN2)
NM_001171087.2:c.1163C>A (CLCN2)	NP_001164558.1:p.Ala388Asp
NM_001171088.2:c.1031C>A (CLCN2)	NP_001164559.1:p.Ala344Asp
NM_001171089.2:c.1163C>A (CLCN2)	NP_001164560.1:p.Ala388Asp
NM_004366.5:c.1163C>A (CLCN2)	NP_004357.3:p.Ala388Asp
XM_006713489.1:c.1163C>A (CLCN2)	XP_006713552.1:p.Ala388Asp
XM_006713490.1:c.5C>A (CLCN2)	XP_006713553.1:p.Ala2Asp
XM_011512401.1:c.1163C>A (CLCN2)	XP_011510703.1:p.Ala388Asp
XM_011512402.1:c.1163C>A (CLCN2)	XP_011510704.1:p.Ala388Asp
XM_006713490.2:c.5C>A (CLCN2)	XP_006713553.1:p.Ala2Asp
XR_001740001.1:n.1287C>A (CLCN2)
XR_001740002.1:n.1287C>A (CLCN2)
NM_004366.6:c.1163C>A (CLCN2) MANE Select	NP_004357.3:p.Ala388Asp
NM_001171087.3:c.1163C>A (CLCN2)	NP_001164558.1:p.Ala388Asp
NM_001171088.3:c.1031C>A (CLCN2)	NP_001164559.1:p.Ala344Asp
NM_001171089.3:c.1163C>A (CLCN2)	NP_001164560.1:p.Ala388Asp