Canonical Allele Identifier: CA1112118161

Gene: CLU

Linked Data

• dbSNP Id: rs1800834270
• gnomAD v3: 8-27607006-C-CT
• gnomAD v4: 8-27607006-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27607007dup , CM000670.2:g.27607007dup	GRCh38
NC_000008.10:g.27464524dup , CM000670.1:g.27464524dup	GRCh37
NC_000008.9:g.27520441dup	NCBI36
NG_027845.1:g.12804dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000316403.15:c.247-483dup MANE Select	ENSP00000315130.10:n.247-483dup
ENST00000316403.14:c.247-483dup	ENSP00000315130.10:n.247-483dup
ENST00000405140.7:c.247-483dup	ENSP00000385419.3:n.247-483dup
ENST00000519742.5:c.247-483dup	ENSP00000431026.1:n.247-483dup
ENST00000520491.5:c.247-483dup	ENSP00000429881.1:n.247-483dup
ENST00000520796.5:c.247-483dup	ENSP00000429336.1:n.247-483dup
ENST00000522299.5:n.315-483dup
ENST00000522413.5:c.247-483dup	ENSP00000428779.1:n.247-483dup
ENST00000523500.5:c.247-483dup	ENSP00000429620.1:n.247-483dup
ENST00000523589.5:c.247-483dup	ENSP00000431070.1:n.247-483dup
ENST00000560566.5:c.280-483dup	ENSP00000453247.1:n.280-483dup
NM_001831.3:c.247-483dup	NP_001822.3:n.247-483dup
NR_038335.1:n.568-483dup
NR_045494.1:n.427-483dup
XM_006716284.1:c.403-483dup	XP_006716347.1:n.403-483dup
XM_006716284.3:c.403-483dup	XP_006716347.1:n.403-483dup
NM_001831.4:c.247-483dup MANE Select	NP_001822.3:n.247-483dup
NR_038335.2:n.502-483dup