Canonical Allele Identifier: CA2842439099

Gene: CLU

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27607067G>A , CM000670.2:g.27607067G>A	GRCh38
NC_000008.10:g.27464584G>A , CM000670.1:g.27464584G>A	GRCh37
NC_000008.9:g.27520501G>A	NCBI36
NG_027845.1:g.12744C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316403.15:c.247-543C>T MANE Select	ENSP00000315130.10:n.247-543C>T
ENST00000316403.14:c.247-543C>T	ENSP00000315130.10:n.247-543C>T
ENST00000405140.7:c.247-543C>T	ENSP00000385419.3:n.247-543C>T
ENST00000519742.5:c.247-543C>T	ENSP00000431026.1:n.247-543C>T
ENST00000520491.5:c.247-543C>T	ENSP00000429881.1:n.247-543C>T
ENST00000520796.5:c.247-543C>T	ENSP00000429336.1:n.247-543C>T
ENST00000522299.5:n.315-543C>T
ENST00000522413.5:c.247-543C>T	ENSP00000428779.1:n.247-543C>T
ENST00000523500.5:c.247-543C>T	ENSP00000429620.1:n.247-543C>T
ENST00000523589.5:c.247-543C>T	ENSP00000431070.1:n.247-543C>T
ENST00000560566.5:c.280-543C>T	ENSP00000453247.1:n.280-543C>T
NM_001831.3:c.247-543C>T	NP_001822.3:n.247-543C>T
NR_038335.1:n.568-543C>T
NR_045494.1:n.427-543C>T
XM_006716284.1:c.403-543C>T	XP_006716347.1:n.403-543C>T
XM_006716284.3:c.403-543C>T	XP_006716347.1:n.403-543C>T
NM_001831.4:c.247-543C>T MANE Select	NP_001822.3:n.247-543C>T
NR_038335.2:n.502-543C>T