Canonical Allele Identifier: CA580671046

Gene: CLU

Linked Data

• dbSNP Id: rs753898068
• gnomAD v2: 8-27464527-C-T
• gnomAD v3: 8-27607010-C-T
• gnomAD v4: 8-27607010-C-T
• MyVariant Identifiers: chr8:g.27464527C>T (hg19) ; chr8:g.27607010C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27607010C>T , CM000670.2:g.27607010C>T	GRCh38
NC_000008.10:g.27464527C>T , CM000670.1:g.27464527C>T	GRCh37
NC_000008.9:g.27520444C>T	NCBI36
NG_027845.1:g.12801G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000316403.15:c.247-486G>A MANE Select	ENSP00000315130.10:n.247-486G>A
ENST00000316403.14:c.247-486G>A	ENSP00000315130.10:n.247-486G>A
ENST00000405140.7:c.247-486G>A	ENSP00000385419.3:n.247-486G>A
ENST00000519742.5:c.247-486G>A	ENSP00000431026.1:n.247-486G>A
ENST00000520491.5:c.247-486G>A	ENSP00000429881.1:n.247-486G>A
ENST00000520796.5:c.247-486G>A	ENSP00000429336.1:n.247-486G>A
ENST00000522299.5:n.315-486G>A
ENST00000522413.5:c.247-486G>A	ENSP00000428779.1:n.247-486G>A
ENST00000523500.5:c.247-486G>A	ENSP00000429620.1:n.247-486G>A
ENST00000523589.5:c.247-486G>A	ENSP00000431070.1:n.247-486G>A
ENST00000560566.5:c.280-486G>A	ENSP00000453247.1:n.280-486G>A
NM_001831.3:c.247-486G>A	NP_001822.3:n.247-486G>A
NR_038335.1:n.568-486G>A
NR_045494.1:n.427-486G>A
XM_006716284.1:c.403-486G>A	XP_006716347.1:n.403-486G>A
XM_006716284.3:c.403-486G>A	XP_006716347.1:n.403-486G>A
NM_001831.4:c.247-486G>A MANE Select	NP_001822.3:n.247-486G>A
NR_038335.2:n.502-486G>A