Canonical Allele Identifier: CA2686690956
Gene: CLU HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27608743_27608749del , CM000670.2:g.27608743_27608749del GRCh38
NC_000008.10:g.27466260_27466266del , CM000670.1:g.27466260_27466266del GRCh37
NC_000008.9:g.27522177_27522183del NCBI36
NG_027845.1:g.11067_11073del

Transcript Alleles

HGVS Amino-acid Change
ENST00000316403.15:c.246+194_246+200del MANE Select ENSP00000315130.10:n.246+194_246+200del
ENST00000316403.14:c.246+194_246+200del ENSP00000315130.10:n.246+194_246+200del
ENST00000405140.7:c.246+194_246+200del ENSP00000385419.3:n.246+194_246+200del
ENST00000518050.1:n.515_521del
ENST00000519742.5:c.246+194_246+200del ENSP00000431026.1:n.246+194_246+200del
ENST00000520491.5:c.246+194_246+200del ENSP00000429881.1:n.246+194_246+200del
ENST00000520796.5:c.246+194_246+200del ENSP00000429336.1:n.246+194_246+200del
ENST00000522299.5:n.314+194_314+200del
ENST00000522413.5:c.246+194_246+200del ENSP00000428779.1:n.246+194_246+200del
ENST00000523500.5:c.246+194_246+200del ENSP00000429620.1:n.246+194_246+200del
ENST00000523589.5:c.246+194_246+200del ENSP00000431070.1:n.246+194_246+200del
ENST00000560566.5:c.279+194_279+200del ENSP00000453247.1:n.279+194_279+200del
NM_001831.3:c.246+194_246+200del NP_001822.3:n.246+194_246+200del
NR_038335.1:n.567+194_567+200del
NR_045494.1:n.426+194_426+200del
XM_006716284.1:c.402+194_402+200del XP_006716347.1:n.402+194_402+200del
XM_006716284.3:c.402+194_402+200del XP_006716347.1:n.402+194_402+200del
NM_001831.4:c.246+194_246+200del MANE Select NP_001822.3:n.246+194_246+200del
NR_038335.2:n.501+194_501+200del