Canonical Allele Identifier: CA2428768909
Gene: CLCN5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50086575A= , CM000685.2:g.50086575A= GRCh38
NC_000023.10:g.49851232A= , CM000685.1:g.49851232A= GRCh37
NC_000023.9:g.49737972A= NCBI36
NG_007159.3:g.168960A=

Transcript Alleles

HGVS Amino-acid change
ENST00000376091.8:c.1262A= MANE Select ENSP00000365259.3:p.Gln421=
ENST00000642383.1:c.512A= ENSP00000496353.1:p.Gln171=
ENST00000642885.1:c.1052A= ENSP00000496632.1:p.Gln351=
ENST00000643129.1:c.1549A=
ENST00000646398.1:c.*437A= ENSP00000495122.1:n.*437A=
ENST00000307367.2:c.1052A= ENSP00000304257.2:p.Gln351=
ENST00000376088.7:c.1262A= ENSP00000365256.3:p.Gln421=
ENST00000376091.7:c.1262A= ENSP00000365259.3:p.Gln421=
ENST00000376108.7:c.1052A= ENSP00000365276.3:p.Gln351=
NM_000084.4:c.1052A= NP_000075.1:p.Gln351=
NM_001127898.3:c.1262A= NP_001121370.1:p.Gln421=
NM_001127899.3:c.1262A= NP_001121371.1:p.Gln421=
NM_001282163.1:c.1112A= NP_001269092.1:p.Gln371=
XM_011543888.1:c.1262A= XP_011542190.1:p.Gln421=
XM_011543889.1:c.1052A= XP_011542191.1:p.Gln351=
XM_017029257.1:c.1274A= XP_016884746.1:p.Gln425=
XM_017029258.1:c.1274A= XP_016884747.1:p.Gln425=
NM_001127898.4:c.1262A= MANE Select NP_001121370.1:p.Gln421=
NM_000084.5:c.1052A= NP_000075.1:p.Gln351=
NM_001127899.4:c.1262A= NP_001121371.1:p.Gln421=
NM_001282163.2:c.1112A= NP_001269092.1:p.Gln371=