Canonical Allele Identifier: CA2695233687
Gene: CLCN5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50086705del , CM000685.2:g.50086705del GRCh38
NC_000023.10:g.49851362del , CM000685.1:g.49851362del GRCh37
NC_000023.9:g.49738102del NCBI36
NG_007159.3:g.169090del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376091.8:c.1392del MANE Select ENSP00000365259.3:p.Leu465TrpfsTer?
ENST00000642383.1:c.642del ENSP00000496353.1:p.Leu215TrpfsTer?
ENST00000642885.1:c.1182del ENSP00000496632.1:p.Leu395TrpfsTer?
ENST00000643129.1:c.1679del
ENST00000646398.1:c.*567del ENSP00000495122.1:n.*567del
ENST00000307367.2:c.1182del ENSP00000304257.2:p.Leu395TrpfsTer?
ENST00000376088.7:c.1392del ENSP00000365256.3:p.Leu465TrpfsTer?
ENST00000376091.7:c.1392del ENSP00000365259.3:p.Leu465TrpfsTer?
ENST00000376108.7:c.1182del ENSP00000365276.3:p.Leu395TrpfsTer?
NM_000084.4:c.1182del NP_000075.1:p.Leu395TrpfsTer?
NM_001127898.3:c.1392del NP_001121370.1:p.Leu465TrpfsTer?
NM_001127899.3:c.1392del NP_001121371.1:p.Leu465TrpfsTer?
NM_001282163.1:c.1242del NP_001269092.1:p.Leu415TrpfsTer?
XM_011543888.1:c.1392del XP_011542190.1:p.Leu465TrpfsTer?
XM_011543889.1:c.1182del XP_011542191.1:p.Leu395TrpfsTer?
XM_017029257.1:c.1404del XP_016884746.1:p.Leu469TrpfsTer?
XM_017029258.1:c.1404del XP_016884747.1:p.Leu469TrpfsTer?
NM_001127898.4:c.1392del MANE Select NP_001121370.1:p.Leu465TrpfsTer?
NM_000084.5:c.1182del NP_000075.1:p.Leu395TrpfsTer?
NM_001127899.4:c.1392del NP_001121371.1:p.Leu465TrpfsTer?
NM_001282163.2:c.1242del NP_001269092.1:p.Leu415TrpfsTer?