Canonical Allele Identifier: CA2428768857
Gene: CLCN5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50086362G= , CM000685.2:g.50086362G= GRCh38
NC_000023.10:g.49851019G= , CM000685.1:g.49851019G= GRCh37
NC_000023.9:g.49737759G= NCBI36
NG_007159.3:g.168747G=

Transcript Alleles

HGVS Amino-acid change
ENST00000376091.8:c.1049G= MANE Select ENSP00000365259.3:p.Arg350=
ENST00000642383.1:c.299G= ENSP00000496353.1:p.Arg100=
ENST00000642885.1:c.839G= ENSP00000496632.1:p.Arg280=
ENST00000643129.1:c.1336G=
ENST00000646398.1:c.*224G= ENSP00000495122.1:n.*224G=
ENST00000307367.2:c.839G= ENSP00000304257.2:p.Arg280=
ENST00000376088.7:c.1049G= ENSP00000365256.3:p.Arg350=
ENST00000376091.7:c.1049G= ENSP00000365259.3:p.Arg350=
ENST00000376108.7:c.839G= ENSP00000365276.3:p.Arg280=
NM_000084.4:c.839G= NP_000075.1:p.Arg280=
NM_001127898.3:c.1049G= NP_001121370.1:p.Arg350=
NM_001127899.3:c.1049G= NP_001121371.1:p.Arg350=
NM_001282163.1:c.899G= NP_001269092.1:p.Arg300=
XM_011543888.1:c.1049G= XP_011542190.1:p.Arg350=
XM_011543889.1:c.839G= XP_011542191.1:p.Arg280=
XM_017029257.1:c.1061G= XP_016884746.1:p.Arg354=
XM_017029258.1:c.1061G= XP_016884747.1:p.Arg354=
NM_001127898.4:c.1049G= MANE Select NP_001121370.1:p.Arg350=
NM_000084.5:c.839G= NP_000075.1:p.Arg280=
NM_001127899.4:c.1049G= NP_001121371.1:p.Arg350=
NM_001282163.2:c.899G= NP_001269092.1:p.Arg300=