Canonical Allele Identifier: CA1772891556

Gene: CLU

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27607056G= , CM000670.2:g.27607056G=	GRCh38
NC_000008.10:g.27464573G= , CM000670.1:g.27464573G=	GRCh37
NC_000008.9:g.27520490G=	NCBI36
NG_027845.1:g.12755C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000316403.15:c.247-532C= MANE Select	ENSP00000315130.10:n.247-532C=
ENST00000316403.14:c.247-532C=	ENSP00000315130.10:n.247-532C=
ENST00000405140.7:c.247-532C=	ENSP00000385419.3:n.247-532C=
ENST00000519742.5:c.247-532C=	ENSP00000431026.1:n.247-532C=
ENST00000520491.5:c.247-532C=	ENSP00000429881.1:n.247-532C=
ENST00000520796.5:c.247-532C=	ENSP00000429336.1:n.247-532C=
ENST00000522299.5:n.315-532C=
ENST00000522413.5:c.247-532C=	ENSP00000428779.1:n.247-532C=
ENST00000523500.5:c.247-532C=	ENSP00000429620.1:n.247-532C=
ENST00000523589.5:c.247-532C=	ENSP00000431070.1:n.247-532C=
ENST00000560566.5:c.280-532C=	ENSP00000453247.1:n.280-532C=
NM_001831.3:c.247-532C=	NP_001822.3:n.247-532C=
NR_038335.1:n.568-532C=
NR_045494.1:n.427-532C=
XM_006716284.1:c.403-532C=	XP_006716347.1:n.403-532C=
XM_006716284.3:c.403-532C=	XP_006716347.1:n.403-532C=
NM_001831.4:c.247-532C= MANE Select	NP_001822.3:n.247-532C=
NR_038335.2:n.502-532C=