Canonical Allele Identifier: CA355452199

Gene: CLCN2 EIF2B5

Linked Data

• dbSNP Id: rs1267172949
• gnomAD v2: 3-184073203-C-T
• gnomAD v4: 3-184355415-C-T
• MyVariant Identifiers: chr3:g.184073203C>T (hg19) ; chr3:g.184355415C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184355415C>T , CM000665.2:g.184355415C>T	GRCh38
NC_000003.11:g.184073203C>T , CM000665.1:g.184073203C>T	GRCh37
NC_000003.10:g.185555897C>T	NCBI36
NG_016422.1:g.11189G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265593.9:c.1285G>A (CLCN2) MANE Select	ENSP00000265593.4:p.Ala429Thr
ENST00000475279.2:c.667G>A (CLCN2)
ENST00000636180.1:c.*261G>A (CLCN2)	ENSP00000490374.1:n.*261G>A
ENST00000636241.1:c.1176G>A (CLCN2)
ENST00000636492.1:c.1168G>A (CLCN2)	ENSP00000490313.1:p.Ala390Thr
ENST00000636658.1:c.546G>A (CLCN2)
ENST00000636661.1:c.*1475G>A (CLCN2)	ENSP00000490764.1:n.*1475G>A
ENST00000637392.1:n.2561G>A (CLCN2)
ENST00000637538.1:c.591G>A (CLCN2)
ENST00000637909.1:c.1091G>A (CLCN2)
ENST00000638134.1:c.1093G>A (CLCN2)
ENST00000265593.8:c.1285G>A (CLCN2)	ENSP00000265593.4:p.Ala429Thr
ENST00000344937.11:c.1285G>A (CLCN2)	ENSP00000345056.7:p.Ala429Thr
ENST00000430397.5:c.228G>A (CLCN2)
ENST00000434054.6:c.1153G>A (CLCN2)	ENSP00000400425.2:p.Ala385Thr
ENST00000444495.1:c.2106+210708C>T (EIF2B5)	ENSP00000409142.1:n.2106+210708C>T
ENST00000457512.1:c.1285G>A (CLCN2)	ENSP00000391928.1:p.Ala429Thr
ENST00000475279.1:n.303G>A (CLCN2)
ENST00000485667.1:n.1292G>A (CLCN2)
NM_001171087.2:c.1285G>A (CLCN2)	NP_001164558.1:p.Ala429Thr
NM_001171088.2:c.1153G>A (CLCN2)	NP_001164559.1:p.Ala385Thr
NM_001171089.2:c.1285G>A (CLCN2)	NP_001164560.1:p.Ala429Thr
NM_004366.5:c.1285G>A (CLCN2)	NP_004357.3:p.Ala429Thr
XM_006713489.1:c.1285G>A (CLCN2)	XP_006713552.1:p.Ala429Thr
XM_006713490.1:c.127G>A (CLCN2)	XP_006713553.1:p.Ala43Thr
XM_011512401.1:c.1285G>A (CLCN2)	XP_011510703.1:p.Ala429Thr
XM_011512402.1:c.1285G>A (CLCN2)	XP_011510704.1:p.Ala429Thr
XM_006713490.2:c.127G>A (CLCN2)	XP_006713553.1:p.Ala43Thr
XR_001740001.1:n.1409G>A (CLCN2)
XR_001740002.1:n.1409G>A (CLCN2)
NM_004366.6:c.1285G>A (CLCN2) MANE Select	NP_004357.3:p.Ala429Thr
NM_001171087.3:c.1285G>A (CLCN2)	NP_001164558.1:p.Ala429Thr
NM_001171088.3:c.1153G>A (CLCN2)	NP_001164559.1:p.Ala385Thr
NM_001171089.3:c.1285G>A (CLCN2)	NP_001164560.1:p.Ala429Thr