Canonical Allele Identifier: CA355452421
Gene: CLCN2 HGNC NCBI
EIF2B5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184355439A>C , CM000665.2:g.184355439A>C GRCh38
NC_000003.11:g.184073227A>C , CM000665.1:g.184073227A>C GRCh37
NC_000003.10:g.185555921A>C NCBI36
NG_016422.1:g.11165T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265593.9:c.1261T>G (CLCN2) MANE Select ENSP00000265593.4:p.Ser421Ala
ENST00000475279.2:c.643T>G (CLCN2)
ENST00000636180.1:c.*237T>G (CLCN2) ENSP00000490374.1:n.*237T>G
ENST00000636241.1:c.1152T>G (CLCN2)
ENST00000636492.1:c.1144T>G (CLCN2) ENSP00000490313.1:p.Ser382Ala
ENST00000636658.1:c.522T>G (CLCN2)
ENST00000636661.1:c.*1451T>G (CLCN2) ENSP00000490764.1:n.*1451T>G
ENST00000637392.1:n.2537T>G (CLCN2)
ENST00000637538.1:c.567T>G (CLCN2)
ENST00000637909.1:c.1067T>G (CLCN2)
ENST00000638134.1:c.1069T>G (CLCN2)
ENST00000265593.8:c.1261T>G (CLCN2) ENSP00000265593.4:p.Ser421Ala
ENST00000344937.11:c.1261T>G (CLCN2) ENSP00000345056.7:p.Ser421Ala
ENST00000430397.5:c.204T>G (CLCN2)
ENST00000434054.6:c.1129T>G (CLCN2) ENSP00000400425.2:p.Ser377Ala
ENST00000444495.1:c.2106+210732A>C (EIF2B5) ENSP00000409142.1:n.2106+210732A>C
ENST00000457512.1:c.1261T>G (CLCN2) ENSP00000391928.1:p.Ser421Ala
ENST00000475279.1:n.279T>G (CLCN2)
ENST00000485667.1:n.1268T>G (CLCN2)
NM_001171087.2:c.1261T>G (CLCN2) NP_001164558.1:p.Ser421Ala
NM_001171088.2:c.1129T>G (CLCN2) NP_001164559.1:p.Ser377Ala
NM_001171089.2:c.1261T>G (CLCN2) NP_001164560.1:p.Ser421Ala
NM_004366.5:c.1261T>G (CLCN2) NP_004357.3:p.Ser421Ala
XM_006713489.1:c.1261T>G (CLCN2) XP_006713552.1:p.Ser421Ala
XM_006713490.1:c.103T>G (CLCN2) XP_006713553.1:p.Ser35Ala
XM_011512401.1:c.1261T>G (CLCN2) XP_011510703.1:p.Ser421Ala
XM_011512402.1:c.1261T>G (CLCN2) XP_011510704.1:p.Ser421Ala
XM_006713490.2:c.103T>G (CLCN2) XP_006713553.1:p.Ser35Ala
XR_001740001.1:n.1385T>G (CLCN2)
XR_001740002.1:n.1385T>G (CLCN2)
NM_004366.6:c.1261T>G (CLCN2) MANE Select NP_004357.3:p.Ser421Ala
NM_001171087.3:c.1261T>G (CLCN2) NP_001164558.1:p.Ser421Ala
NM_001171088.3:c.1129T>G (CLCN2) NP_001164559.1:p.Ser377Ala
NM_001171089.3:c.1261T>G (CLCN2) NP_001164560.1:p.Ser421Ala