Canonical Allele Identifier: CA355447162

Gene: CLCN2 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.184069894C>T (hg19) ; chr3:g.184352106C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184352106C>T , CM000665.2:g.184352106C>T	GRCh38
NC_000003.11:g.184069894C>T , CM000665.1:g.184069894C>T	GRCh37
NC_000003.10:g.185552588C>T	NCBI36
NG_016422.1:g.14498G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265593.9:c.2322G>A (CLCN2) MANE Select	ENSP00000265593.4:p.Trp774Ter
ENST00000636180.1:c.*1220G>A (CLCN2)	ENSP00000490374.1:n.*1220G>A
ENST00000636661.1:c.*2632G>A (CLCN2)	ENSP00000490764.1:n.*2632G>A
ENST00000637392.1:n.3864G>A (CLCN2)
ENST00000637909.1:c.2128G>A (CLCN2)
ENST00000265593.8:c.2322G>A (CLCN2)	ENSP00000265593.4:p.Trp774Ter
ENST00000344937.11:c.2271G>A (CLCN2)	ENSP00000345056.7:p.Trp757Ter
ENST00000430397.5:c.1177+187G>A (CLCN2)
ENST00000434054.6:c.2190G>A (CLCN2)	ENSP00000400425.2:p.Trp730Ter
ENST00000444495.1:c.2106+207399C>T (EIF2B5)	ENSP00000409142.1:n.2106+207399C>T
ENST00000457512.1:c.2322G>A (CLCN2)	ENSP00000391928.1:p.Trp774Ter
NM_001171087.2:c.2271G>A (CLCN2)	NP_001164558.1:p.Trp757Ter
NM_001171088.2:c.2190G>A (CLCN2)	NP_001164559.1:p.Trp730Ter
NM_001171089.2:c.2322G>A (CLCN2)	NP_001164560.1:p.Trp774Ter
NM_004366.5:c.2322G>A (CLCN2)	NP_004357.3:p.Trp774Ter
XM_006713489.1:c.2310+187G>A (CLCN2)	XP_006713552.1:n.2310+187G>A
XM_006713490.1:c.1164G>A (CLCN2)	XP_006713553.1:p.Trp388Ter
XM_011512401.1:c.2322G>A (CLCN2)	XP_011510703.1:p.Trp774Ter
XM_006713490.2:c.1164G>A (CLCN2)	XP_006713553.1:p.Trp388Ter
XR_001740001.1:n.2502G>A (CLCN2)
XR_001740002.1:n.2490+187G>A (CLCN2)
NM_004366.6:c.2322G>A (CLCN2) MANE Select	NP_004357.3:p.Trp774Ter
NM_001171087.3:c.2271G>A (CLCN2)	NP_001164558.1:p.Trp757Ter
NM_001171088.3:c.2190G>A (CLCN2)	NP_001164559.1:p.Trp730Ter
NM_001171089.3:c.2322G>A (CLCN2)	NP_001164560.1:p.Trp774Ter