Canonical Allele Identifier: CA2779506983

Gene: CLU

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27607204del , CM000670.2:g.27607204del	GRCh38
NC_000008.10:g.27464721del , CM000670.1:g.27464721del	GRCh37
NC_000008.9:g.27520638del	NCBI36
NG_027845.1:g.12608del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316403.15:c.247-679del MANE Select	ENSP00000315130.10:n.247-679del
ENST00000316403.14:c.247-679del	ENSP00000315130.10:n.247-679del
ENST00000405140.7:c.247-679del	ENSP00000385419.3:n.247-679del
ENST00000519742.5:c.247-679del	ENSP00000431026.1:n.247-679del
ENST00000520491.5:c.247-679del	ENSP00000429881.1:n.247-679del
ENST00000520796.5:c.247-679del	ENSP00000429336.1:n.247-679del
ENST00000522299.5:n.315-679del
ENST00000522413.5:c.247-679del	ENSP00000428779.1:n.247-679del
ENST00000523500.5:c.247-679del	ENSP00000429620.1:n.247-679del
ENST00000523589.5:c.247-679del	ENSP00000431070.1:n.247-679del
ENST00000560566.5:c.280-679del	ENSP00000453247.1:n.280-679del
NM_001831.3:c.247-679del	NP_001822.3:n.247-679del
NR_038335.1:n.568-679del
NR_045494.1:n.427-679del
XM_006716284.1:c.403-679del	XP_006716347.1:n.403-679del
XM_006716284.3:c.403-679del	XP_006716347.1:n.403-679del
NM_001831.4:c.247-679del MANE Select	NP_001822.3:n.247-679del
NR_038335.2:n.502-679del