Canonical Allele Identifier: CA355451900
Gene: CLCN2 HGNC NCBI
EIF2B5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184355378A>T , CM000665.2:g.184355378A>T GRCh38
NC_000003.11:g.184073166A>T , CM000665.1:g.184073166A>T GRCh37
NC_000003.10:g.185555860A>T NCBI36
NG_016422.1:g.11226T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265593.9:c.1322T>A (CLCN2) MANE Select ENSP00000265593.4:p.Met441Lys
ENST00000475279.2:c.704T>A (CLCN2)
ENST00000636180.1:c.*298T>A (CLCN2) ENSP00000490374.1:n.*298T>A
ENST00000636241.1:c.1213T>A (CLCN2)
ENST00000636492.1:c.1205T>A (CLCN2) ENSP00000490313.1:p.Met402Lys
ENST00000636658.1:c.583T>A (CLCN2)
ENST00000636661.1:c.*1512T>A (CLCN2) ENSP00000490764.1:n.*1512T>A
ENST00000637392.1:n.2598T>A (CLCN2)
ENST00000637538.1:c.628T>A (CLCN2)
ENST00000637909.1:c.1128T>A (CLCN2)
ENST00000638134.1:c.1130T>A (CLCN2)
ENST00000265593.8:c.1322T>A (CLCN2) ENSP00000265593.4:p.Met441Lys
ENST00000344937.11:c.1322T>A (CLCN2) ENSP00000345056.7:p.Met441Lys
ENST00000430397.5:c.265T>A (CLCN2)
ENST00000434054.6:c.1190T>A (CLCN2) ENSP00000400425.2:p.Met397Lys
ENST00000444495.1:c.2106+210671A>T (EIF2B5) ENSP00000409142.1:n.2106+210671A>T
ENST00000457512.1:c.1322T>A (CLCN2) ENSP00000391928.1:p.Met441Lys
ENST00000485667.1:n.1329T>A (CLCN2)
NM_001171087.2:c.1322T>A (CLCN2) NP_001164558.1:p.Met441Lys
NM_001171088.2:c.1190T>A (CLCN2) NP_001164559.1:p.Met397Lys
NM_001171089.2:c.1322T>A (CLCN2) NP_001164560.1:p.Met441Lys
NM_004366.5:c.1322T>A (CLCN2) NP_004357.3:p.Met441Lys
XM_006713489.1:c.1322T>A (CLCN2) XP_006713552.1:p.Met441Lys
XM_006713490.1:c.164T>A (CLCN2) XP_006713553.1:p.Met55Lys
XM_011512401.1:c.1322T>A (CLCN2) XP_011510703.1:p.Met441Lys
XM_011512402.1:c.1322T>A (CLCN2) XP_011510704.1:p.Met441Lys
XM_006713490.2:c.164T>A (CLCN2) XP_006713553.1:p.Met55Lys
XR_001740001.1:n.1446T>A (CLCN2)
XR_001740002.1:n.1446T>A (CLCN2)
NM_004366.6:c.1322T>A (CLCN2) MANE Select NP_004357.3:p.Met441Lys
NM_001171087.3:c.1322T>A (CLCN2) NP_001164558.1:p.Met441Lys
NM_001171088.3:c.1190T>A (CLCN2) NP_001164559.1:p.Met397Lys
NM_001171089.3:c.1322T>A (CLCN2) NP_001164560.1:p.Met441Lys