Canonical Allele Identifier: CA174274365

Gene: CLU

Linked Data

• dbSNP Id: rs567557842
• gnomAD v3: 8-27607009-A-G
• gnomAD v4: 8-27607009-A-G
• MyVariant Identifiers: chr8:g.27464526A>G (hg19) ; chr8:g.27607009A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27607009A>G , CM000670.2:g.27607009A>G	GRCh38
NC_000008.10:g.27464526A>G , CM000670.1:g.27464526A>G	GRCh37
NC_000008.9:g.27520443A>G	NCBI36
NG_027845.1:g.12802T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000316403.15:c.247-485T>C MANE Select	ENSP00000315130.10:n.247-485T>C
ENST00000316403.14:c.247-485T>C	ENSP00000315130.10:n.247-485T>C
ENST00000405140.7:c.247-485T>C	ENSP00000385419.3:n.247-485T>C
ENST00000519742.5:c.247-485T>C	ENSP00000431026.1:n.247-485T>C
ENST00000520491.5:c.247-485T>C	ENSP00000429881.1:n.247-485T>C
ENST00000520796.5:c.247-485T>C	ENSP00000429336.1:n.247-485T>C
ENST00000522299.5:n.315-485T>C
ENST00000522413.5:c.247-485T>C	ENSP00000428779.1:n.247-485T>C
ENST00000523500.5:c.247-485T>C	ENSP00000429620.1:n.247-485T>C
ENST00000523589.5:c.247-485T>C	ENSP00000431070.1:n.247-485T>C
ENST00000560566.5:c.280-485T>C	ENSP00000453247.1:n.280-485T>C
NM_001831.3:c.247-485T>C	NP_001822.3:n.247-485T>C
NR_038335.1:n.568-485T>C
NR_045494.1:n.427-485T>C
XM_006716284.1:c.403-485T>C	XP_006716347.1:n.403-485T>C
XM_006716284.3:c.403-485T>C	XP_006716347.1:n.403-485T>C
NM_001831.4:c.247-485T>C MANE Select	NP_001822.3:n.247-485T>C
NR_038335.2:n.502-485T>C