Canonical Allele Identifier: CA516678505
Gene: CLCN5 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.49851213C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50086556C>A , CM000685.2:g.50086556C>A GRCh38
NC_000023.10:g.49851213C>A , CM000685.1:g.49851213C>A GRCh37
NC_000023.9:g.49737953C>A NCBI36
NG_007159.3:g.168941C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376091.8:c.1243C>A MANE Select ENSP00000365259.3:p.Arg415=
ENST00000642383.1:c.493C>A ENSP00000496353.1:p.Arg165=
ENST00000642885.1:c.1033C>A ENSP00000496632.1:p.Arg345=
ENST00000643129.1:c.1530C>A
ENST00000646398.1:c.*418C>A ENSP00000495122.1:n.*418C>A
ENST00000307367.2:c.1033C>A ENSP00000304257.2:p.Arg345=
ENST00000376088.7:c.1243C>A ENSP00000365256.3:p.Arg415=
ENST00000376091.7:c.1243C>A ENSP00000365259.3:p.Arg415=
ENST00000376108.7:c.1033C>A ENSP00000365276.3:p.Arg345=
NM_000084.4:c.1033C>A NP_000075.1:p.Arg345=
NM_001127898.3:c.1243C>A NP_001121370.1:p.Arg415=
NM_001127899.3:c.1243C>A NP_001121371.1:p.Arg415=
NM_001282163.1:c.1093C>A NP_001269092.1:p.Arg365=
XM_011543888.1:c.1243C>A XP_011542190.1:p.Arg415=
XM_011543889.1:c.1033C>A XP_011542191.1:p.Arg345=
XM_017029257.1:c.1255C>A XP_016884746.1:p.Arg419=
XM_017029258.1:c.1255C>A XP_016884747.1:p.Arg419=
NM_001127898.4:c.1243C>A MANE Select NP_001121370.1:p.Arg415=
NM_000084.5:c.1033C>A NP_000075.1:p.Arg345=
NM_001127899.4:c.1243C>A NP_001121371.1:p.Arg415=
NM_001282163.2:c.1093C>A NP_001269092.1:p.Arg365=