Canonical Allele Identifier: CA437167328

Gene: CLCN2 EIF2B5

Linked Data

• gnomAD v4: 3-184355374-C-T
• MyVariant Identifiers: chr3:g.184073162C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184355374C>T , CM000665.2:g.184355374C>T	GRCh38
NC_000003.11:g.184073162C>T , CM000665.1:g.184073162C>T	GRCh37
NC_000003.10:g.185555856C>T	NCBI36
NG_016422.1:g.11230G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265593.9:c.1326G>A (CLCN2) MANE Select	ENSP00000265593.4:p.Lys442=
ENST00000475279.2:c.708G>A (CLCN2)
ENST00000636180.1:c.*302G>A (CLCN2)	ENSP00000490374.1:n.*302G>A
ENST00000636241.1:c.1217G>A (CLCN2)
ENST00000636492.1:c.1209G>A (CLCN2)	ENSP00000490313.1:p.Lys403=
ENST00000636658.1:c.587G>A (CLCN2)
ENST00000636661.1:c.*1516G>A (CLCN2)	ENSP00000490764.1:n.*1516G>A
ENST00000637392.1:n.2602G>A (CLCN2)
ENST00000637538.1:c.632G>A (CLCN2)
ENST00000637909.1:c.1132G>A (CLCN2)
ENST00000638134.1:c.1134G>A (CLCN2)
ENST00000265593.8:c.1326G>A (CLCN2)	ENSP00000265593.4:p.Lys442=
ENST00000344937.11:c.1326G>A (CLCN2)	ENSP00000345056.7:p.Lys442=
ENST00000430397.5:c.269G>A (CLCN2)
ENST00000434054.6:c.1194G>A (CLCN2)	ENSP00000400425.2:p.Lys398=
ENST00000444495.1:c.2106+210667C>T (EIF2B5)	ENSP00000409142.1:n.2106+210667C>T
ENST00000457512.1:c.1326G>A (CLCN2)	ENSP00000391928.1:p.Lys442=
ENST00000485667.1:n.1333G>A (CLCN2)
NM_001171087.2:c.1326G>A (CLCN2)	NP_001164558.1:p.Lys442=
NM_001171088.2:c.1194G>A (CLCN2)	NP_001164559.1:p.Lys398=
NM_001171089.2:c.1326G>A (CLCN2)	NP_001164560.1:p.Lys442=
NM_004366.5:c.1326G>A (CLCN2)	NP_004357.3:p.Lys442=
XM_006713489.1:c.1326G>A (CLCN2)	XP_006713552.1:p.Lys442=
XM_006713490.1:c.168G>A (CLCN2)	XP_006713553.1:p.Lys56=
XM_011512401.1:c.1326G>A (CLCN2)	XP_011510703.1:p.Lys442=
XM_011512402.1:c.1326G>A (CLCN2)	XP_011510704.1:p.Lys442=
XM_006713490.2:c.168G>A (CLCN2)	XP_006713553.1:p.Lys56=
XR_001740001.1:n.1450G>A (CLCN2)
XR_001740002.1:n.1450G>A (CLCN2)
NM_004366.6:c.1326G>A (CLCN2) MANE Select	NP_004357.3:p.Lys442=
NM_001171087.3:c.1326G>A (CLCN2)	NP_001164558.1:p.Lys442=
NM_001171088.3:c.1194G>A (CLCN2)	NP_001164559.1:p.Lys398=
NM_001171089.3:c.1326G>A (CLCN2)	NP_001164560.1:p.Lys442=