Canonical Allele Identifier: CA1772891675

Gene: CLU

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27607210A= , CM000670.2:g.27607210A=	GRCh38
NC_000008.10:g.27464727A= , CM000670.1:g.27464727A=	GRCh37
NC_000008.9:g.27520644A=	NCBI36
NG_027845.1:g.12601T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316403.15:c.247-686T= MANE Select	ENSP00000315130.10:n.247-686T=
ENST00000316403.14:c.247-686T=	ENSP00000315130.10:n.247-686T=
ENST00000405140.7:c.247-686T=	ENSP00000385419.3:n.247-686T=
ENST00000519742.5:c.247-686T=	ENSP00000431026.1:n.247-686T=
ENST00000520491.5:c.247-686T=	ENSP00000429881.1:n.247-686T=
ENST00000520796.5:c.247-686T=	ENSP00000429336.1:n.247-686T=
ENST00000522299.5:n.315-686T=
ENST00000522413.5:c.247-686T=	ENSP00000428779.1:n.247-686T=
ENST00000523500.5:c.247-686T=	ENSP00000429620.1:n.247-686T=
ENST00000523589.5:c.247-686T=	ENSP00000431070.1:n.247-686T=
ENST00000560566.5:c.280-686T=	ENSP00000453247.1:n.280-686T=
NM_001831.3:c.247-686T=	NP_001822.3:n.247-686T=
NR_038335.1:n.568-686T=
NR_045494.1:n.427-686T=
XM_006716284.1:c.403-686T=	XP_006716347.1:n.403-686T=
XM_006716284.3:c.403-686T=	XP_006716347.1:n.403-686T=
NM_001831.4:c.247-686T= MANE Select	NP_001822.3:n.247-686T=
NR_038335.2:n.502-686T=