Canonical Allele Identifier: CA1772891462
Gene: CLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27606939_27606963delinsTGCCTCCTGGCGTGCAAAGGGAATG , CM000670.2:g.27606939_27606963delinsTGCCTCCTGGCGTGCAAAGGGAATG GRCh38
NC_000008.10:g.27464456_27464480delinsTGCCTCCTGGCGTGCAAAGGGAATG , CM000670.1:g.27464456_27464480delinsTGCCTCCTGGCGTGCAAAGGGAATG GRCh37
NC_000008.9:g.27520373_27520397delinsTGCCTCCTGGCGTGCAAAGGGAATG NCBI36
NG_027845.1:g.12848_12872delinsCATTCCCTTTGCACGCCAGGAGGCA

Transcript Alleles

HGVS Amino-acid change
ENST00000316403.15:c.247-439_247-415delinsCATTCCCTTTGCACGCCAGGAGGCA MANE Select ENSP00000315130.10:n.247-439_247-415delinsCATTCCCTTTGCACGCCAG...
ENST00000316403.14:c.247-439_247-415delinsCATTCCCTTTGCACGCCAGGAGGCA ENSP00000315130.10:n.247-439_247-415delinsCATTCCCTTTGCACGCCAG...
ENST00000405140.7:c.247-439_247-415delinsCATTCCCTTTGCACGCCAGGAGGCA ENSP00000385419.3:n.247-439_247-415delinsCATTCCCTTTGCACGCCAGG...
ENST00000519742.5:c.247-439_247-415delinsCATTCCCTTTGCACGCCAGGAGGCA ENSP00000431026.1:n.247-439_247-415delinsCATTCCCTTTGCACGCCAGG...
ENST00000520491.5:c.247-439_247-415delinsCATTCCCTTTGCACGCCAGGAGGCA ENSP00000429881.1:n.247-439_247-415delinsCATTCCCTTTGCACGCCAGG...
ENST00000520796.5:c.247-439_247-415delinsCATTCCCTTTGCACGCCAGGAGGCA ENSP00000429336.1:n.247-439_247-415delinsCATTCCCTTTGCACGCCAGG...
ENST00000522299.5:n.315-439_315-415delinsCATTCCCTTTGCACGCCAGGAGGCA
ENST00000522413.5:c.247-439_247-415delinsCATTCCCTTTGCACGCCAGGAGGCA ENSP00000428779.1:n.247-439_247-415delinsCATTCCCTTTGCACGCCAGG...
ENST00000523500.5:c.247-439_247-415delinsCATTCCCTTTGCACGCCAGGAGGCA ENSP00000429620.1:n.247-439_247-415delinsCATTCCCTTTGCACGCCAGG...
ENST00000523589.5:c.247-439_247-415delinsCATTCCCTTTGCACGCCAGGAGGCA ENSP00000431070.1:n.247-439_247-415delinsCATTCCCTTTGCACGCCAGG...
ENST00000560566.5:c.280-439_280-415delinsCATTCCCTTTGCACGCCAGGAGGCA ENSP00000453247.1:n.280-439_280-415delinsCATTCCCTTTGCACGCCAGG...
NM_001831.3:c.247-439_247-415delinsCATTCCCTTTGCACGCCAGGAGGCA NP_001822.3:n.247-439_247-415delinsCATTCCCTTTGCACGCCAGGAGGCA
NR_038335.1:n.568-439_568-415delinsCATTCCCTTTGCACGCCAGGAGGCA
NR_045494.1:n.427-439_427-415delinsCATTCCCTTTGCACGCCAGGAGGCA
XM_006716284.1:c.403-439_403-415delinsCATTCCCTTTGCACGCCAGGAGGCA XP_006716347.1:n.403-439_403-415delinsCATTCCCTTTGCACGCCAGGAGG...
XM_006716284.3:c.403-439_403-415delinsCATTCCCTTTGCACGCCAGGAGGCA XP_006716347.1:n.403-439_403-415delinsCATTCCCTTTGCACGCCAGGAGG...
NM_001831.4:c.247-439_247-415delinsCATTCCCTTTGCACGCCAGGAGGCA MANE Select NP_001822.3:n.247-439_247-415delinsCATTCCCTTTGCACGCCAGGAGGCA
NR_038335.2:n.502-439_502-415delinsCATTCCCTTTGCACGCCAGGAGGCA