Canonical Allele Identifier: CA2693737036
Gene: CLCN5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50086149_50086150insAAT , CM000685.2:g.50086149_50086150insAAT GRCh38
NC_000023.10:g.49850806_49850807insAAT , CM000685.1:g.49850806_49850807insAAT GRCh37
NC_000023.9:g.49737546_49737547insAAT NCBI36
NG_007159.3:g.168534_168535insAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000376091.8:c.1014+89_1014+90insAAT MANE Select ENSP00000365259.3:n.1014+89_1014+90insAAT
ENST00000642383.1:c.264+89_264+90insAAT ENSP00000496353.1:n.264+89_264+90insAAT
ENST00000642885.1:c.804+89_804+90insAAT ENSP00000496632.1:n.804+89_804+90insAAT
ENST00000643129.1:c.1301+89_1301+90insAAT
ENST00000646398.1:c.*189+89_*189+90insAAT ENSP00000495122.1:n.*189+89_*189+90insAAT
ENST00000307367.2:c.804+89_804+90insAAT ENSP00000304257.2:n.804+89_804+90insAAT
ENST00000376088.7:c.1014+89_1014+90insAAT ENSP00000365256.3:n.1014+89_1014+90insAAT
ENST00000376091.7:c.1014+89_1014+90insAAT ENSP00000365259.3:n.1014+89_1014+90insAAT
ENST00000376108.7:c.804+89_804+90insAAT ENSP00000365276.3:n.804+89_804+90insAAT
NM_000084.4:c.804+89_804+90insAAT NP_000075.1:n.804+89_804+90insAAT
NM_001127898.3:c.1014+89_1014+90insAAT NP_001121370.1:n.1014+89_1014+90insAAT
NM_001127899.3:c.1014+89_1014+90insAAT NP_001121371.1:n.1014+89_1014+90insAAT
NM_001282163.1:c.864+89_864+90insAAT NP_001269092.1:n.864+89_864+90insAAT
XM_011543888.1:c.1014+89_1014+90insAAT XP_011542190.1:n.1014+89_1014+90insAAT
XM_011543889.1:c.804+89_804+90insAAT XP_011542191.1:n.804+89_804+90insAAT
XM_017029257.1:c.1026+89_1026+90insAAT XP_016884746.1:n.1026+89_1026+90insAAT
XM_017029258.1:c.1026+89_1026+90insAAT XP_016884747.1:n.1026+89_1026+90insAAT
NM_001127898.4:c.1014+89_1014+90insAAT MANE Select NP_001121370.1:n.1014+89_1014+90insAAT
NM_000084.5:c.804+89_804+90insAAT NP_000075.1:n.804+89_804+90insAAT
NM_001127899.4:c.1014+89_1014+90insAAT NP_001121371.1:n.1014+89_1014+90insAAT
NM_001282163.2:c.864+89_864+90insAAT NP_001269092.1:n.864+89_864+90insAAT