Canonical Allele Identifier: CA2428764155
Gene: CLCN5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50072460T= , CM000685.2:g.50072460T= GRCh38
NC_000023.10:g.49837115T= , CM000685.1:g.49837115T= GRCh37
NC_000023.9:g.49723855T= NCBI36
NG_007159.3:g.154845T=

Transcript Alleles

HGVS Amino-acid change
ENST00000376091.8:c.316-29T= MANE Select ENSP00000365259.3:n.316-29T=
ENST00000642885.1:c.106-29T= ENSP00000496632.1:n.106-29T=
ENST00000643129.1:c.603-29T=
ENST00000646398.1:c.106-29T= ENSP00000495122.1:n.106-29T=
ENST00000307367.2:c.106-29T= ENSP00000304257.2:n.106-29T=
ENST00000376088.7:c.316-29T= ENSP00000365256.3:n.316-29T=
ENST00000376091.7:c.316-29T= ENSP00000365259.3:n.316-29T=
ENST00000376108.7:c.106-29T= ENSP00000365276.3:n.106-29T=
NM_000084.4:c.106-29T= NP_000075.1:n.106-29T=
NM_001127898.3:c.316-29T= NP_001121370.1:n.316-29T=
NM_001127899.3:c.316-29T= NP_001121371.1:n.316-29T=
NM_001282163.1:c.166-29T= NP_001269092.1:n.166-29T=
XM_011543888.1:c.316-29T= XP_011542190.1:n.316-29T=
XM_011543889.1:c.106-29T= XP_011542191.1:n.106-29T=
XM_017029257.1:c.328-29T= XP_016884746.1:n.328-29T=
XM_017029258.1:c.328-29T= XP_016884747.1:n.328-29T=
NM_001127898.4:c.316-29T= MANE Select NP_001121370.1:n.316-29T=
NM_000084.5:c.106-29T= NP_000075.1:n.106-29T=
NM_001127899.4:c.316-29T= NP_001121371.1:n.316-29T=
NM_001282163.2:c.166-29T= NP_001269092.1:n.166-29T=