Canonical Allele Identifier: CA580671057

Gene: CLU

Linked Data

• dbSNP Id: rs1468397898
• gnomAD v2: 8-27464718-G-C
• gnomAD v3: 8-27607201-G-C
• gnomAD v4: 8-27607201-G-C
• MyVariant Identifiers: chr8:g.27464718G>C (hg19) ; chr8:g.27607201G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27607201G>C , CM000670.2:g.27607201G>C	GRCh38
NC_000008.10:g.27464718G>C , CM000670.1:g.27464718G>C	GRCh37
NC_000008.9:g.27520635G>C	NCBI36
NG_027845.1:g.12610C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316403.15:c.247-677C>G MANE Select	ENSP00000315130.10:n.247-677C>G
ENST00000316403.14:c.247-677C>G	ENSP00000315130.10:n.247-677C>G
ENST00000405140.7:c.247-677C>G	ENSP00000385419.3:n.247-677C>G
ENST00000519742.5:c.247-677C>G	ENSP00000431026.1:n.247-677C>G
ENST00000520491.5:c.247-677C>G	ENSP00000429881.1:n.247-677C>G
ENST00000520796.5:c.247-677C>G	ENSP00000429336.1:n.247-677C>G
ENST00000522299.5:n.315-677C>G
ENST00000522413.5:c.247-677C>G	ENSP00000428779.1:n.247-677C>G
ENST00000523500.5:c.247-677C>G	ENSP00000429620.1:n.247-677C>G
ENST00000523589.5:c.247-677C>G	ENSP00000431070.1:n.247-677C>G
ENST00000560566.5:c.280-677C>G	ENSP00000453247.1:n.280-677C>G
NM_001831.3:c.247-677C>G	NP_001822.3:n.247-677C>G
NR_038335.1:n.568-677C>G
NR_045494.1:n.427-677C>G
XM_006716284.1:c.403-677C>G	XP_006716347.1:n.403-677C>G
XM_006716284.3:c.403-677C>G	XP_006716347.1:n.403-677C>G
NM_001831.4:c.247-677C>G MANE Select	NP_001822.3:n.247-677C>G
NR_038335.2:n.502-677C>G