Canonical Allele Identifier: CA355452574

Gene: CLCN2 EIF2B5

Linked Data

• dbSNP Id: rs1162900298
• gnomAD v2: 3-184073253-A-G
• gnomAD v4: 3-184355465-A-G
• MyVariant Identifiers: chr3:g.184073253A>G (hg19) ; chr3:g.184355465A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184355465A>G , CM000665.2:g.184355465A>G	GRCh38
NC_000003.11:g.184073253A>G , CM000665.1:g.184073253A>G	GRCh37
NC_000003.10:g.185555947A>G	NCBI36
NG_016422.1:g.11139T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265593.9:c.1235T>C (CLCN2) MANE Select	ENSP00000265593.4:p.Val412Ala
ENST00000475279.2:c.617T>C (CLCN2)
ENST00000636180.1:c.*211T>C (CLCN2)	ENSP00000490374.1:n.*211T>C
ENST00000636241.1:c.1126T>C (CLCN2)
ENST00000636492.1:c.1118T>C (CLCN2)	ENSP00000490313.1:p.Val373Ala
ENST00000636658.1:c.496T>C (CLCN2)
ENST00000636661.1:c.*1425T>C (CLCN2)	ENSP00000490764.1:n.*1425T>C
ENST00000637392.1:n.2511T>C (CLCN2)
ENST00000637538.1:c.541T>C (CLCN2)
ENST00000637909.1:c.1041T>C (CLCN2)
ENST00000638134.1:c.1043T>C (CLCN2)
ENST00000265593.8:c.1235T>C (CLCN2)	ENSP00000265593.4:p.Val412Ala
ENST00000344937.11:c.1235T>C (CLCN2)	ENSP00000345056.7:p.Val412Ala
ENST00000430397.5:c.178T>C (CLCN2)
ENST00000434054.6:c.1103T>C (CLCN2)	ENSP00000400425.2:p.Val368Ala
ENST00000444495.1:c.2106+210758A>G (EIF2B5)	ENSP00000409142.1:n.2106+210758A>G
ENST00000457512.1:c.1235T>C (CLCN2)	ENSP00000391928.1:p.Val412Ala
ENST00000475279.1:n.253T>C (CLCN2)
ENST00000485667.1:n.1242T>C (CLCN2)
NM_001171087.2:c.1235T>C (CLCN2)	NP_001164558.1:p.Val412Ala
NM_001171088.2:c.1103T>C (CLCN2)	NP_001164559.1:p.Val368Ala
NM_001171089.2:c.1235T>C (CLCN2)	NP_001164560.1:p.Val412Ala
NM_004366.5:c.1235T>C (CLCN2)	NP_004357.3:p.Val412Ala
XM_006713489.1:c.1235T>C (CLCN2)	XP_006713552.1:p.Val412Ala
XM_006713490.1:c.77T>C (CLCN2)	XP_006713553.1:p.Val26Ala
XM_011512401.1:c.1235T>C (CLCN2)	XP_011510703.1:p.Val412Ala
XM_011512402.1:c.1235T>C (CLCN2)	XP_011510704.1:p.Val412Ala
XM_006713490.2:c.77T>C (CLCN2)	XP_006713553.1:p.Val26Ala
XR_001740001.1:n.1359T>C (CLCN2)
XR_001740002.1:n.1359T>C (CLCN2)
NM_004366.6:c.1235T>C (CLCN2) MANE Select	NP_004357.3:p.Val412Ala
NM_001171087.3:c.1235T>C (CLCN2)	NP_001164558.1:p.Val412Ala
NM_001171088.3:c.1103T>C (CLCN2)	NP_001164559.1:p.Val368Ala
NM_001171089.3:c.1235T>C (CLCN2)	NP_001164560.1:p.Val412Ala