Canonical Allele Identifier: CA1425984315
Gene: CLCN2 HGNC NCBI
EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184355423G= , CM000665.2:g.184355423G= GRCh38
NC_000003.11:g.184073211G= , CM000665.1:g.184073211G= GRCh37
NC_000003.10:g.185555905G= NCBI36
NG_016422.1:g.11181C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265593.9:c.1277C= (CLCN2) MANE Select ENSP00000265593.4:p.Pro426=
ENST00000475279.2:c.659C= (CLCN2)
ENST00000636180.1:c.*253C= (CLCN2) ENSP00000490374.1:n.*253C=
ENST00000636241.1:c.1168C= (CLCN2)
ENST00000636492.1:c.1160C= (CLCN2) ENSP00000490313.1:p.Pro387=
ENST00000636658.1:c.538C= (CLCN2)
ENST00000636661.1:c.*1467C= (CLCN2) ENSP00000490764.1:n.*1467C=
ENST00000637392.1:n.2553C= (CLCN2)
ENST00000637538.1:c.583C= (CLCN2)
ENST00000637909.1:c.1083C= (CLCN2)
ENST00000638134.1:c.1085C= (CLCN2)
ENST00000265593.8:c.1277C= (CLCN2) ENSP00000265593.4:p.Pro426=
ENST00000344937.11:c.1277C= (CLCN2) ENSP00000345056.7:p.Pro426=
ENST00000430397.5:c.220C= (CLCN2)
ENST00000434054.6:c.1145C= (CLCN2) ENSP00000400425.2:p.Pro382=
ENST00000444495.1:c.2106+210716G= (EIF2B5) ENSP00000409142.1:n.2106+210716G=
ENST00000457512.1:c.1277C= (CLCN2) ENSP00000391928.1:p.Pro426=
ENST00000475279.1:n.295C= (CLCN2)
ENST00000485667.1:n.1284C= (CLCN2)
NM_001171087.2:c.1277C= (CLCN2) NP_001164558.1:p.Pro426=
NM_001171088.2:c.1145C= (CLCN2) NP_001164559.1:p.Pro382=
NM_001171089.2:c.1277C= (CLCN2) NP_001164560.1:p.Pro426=
NM_004366.5:c.1277C= (CLCN2) NP_004357.3:p.Pro426=
XM_006713489.1:c.1277C= (CLCN2) XP_006713552.1:p.Pro426=
XM_006713490.1:c.119C= (CLCN2) XP_006713553.1:p.Pro40=
XM_011512401.1:c.1277C= (CLCN2) XP_011510703.1:p.Pro426=
XM_011512402.1:c.1277C= (CLCN2) XP_011510704.1:p.Pro426=
XM_006713490.2:c.119C= (CLCN2) XP_006713553.1:p.Pro40=
XR_001740001.1:n.1401C= (CLCN2)
XR_001740002.1:n.1401C= (CLCN2)
NM_004366.6:c.1277C= (CLCN2) MANE Select NP_004357.3:p.Pro426=
NM_001171087.3:c.1277C= (CLCN2) NP_001164558.1:p.Pro426=
NM_001171088.3:c.1145C= (CLCN2) NP_001164559.1:p.Pro382=
NM_001171089.3:c.1277C= (CLCN2) NP_001164560.1:p.Pro426=