Canonical Allele Identifier: CA174275359

Gene: CLU

Linked Data

• dbSNP Id: rs949780019
• gnomAD v3: 8-27608605-A-G
• gnomAD v4: 8-27608605-A-G
• MyVariant Identifiers: chr8:g.27466122A>G (hg19) ; chr8:g.27608605A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27608605A>G , CM000670.2:g.27608605A>G	GRCh38
NC_000008.10:g.27466122A>G , CM000670.1:g.27466122A>G	GRCh37
NC_000008.9:g.27522039A>G	NCBI36
NG_027845.1:g.11206T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316403.15:c.246+333T>C MANE Select	ENSP00000315130.10:n.246+333T>C
ENST00000316403.14:c.246+333T>C	ENSP00000315130.10:n.246+333T>C
ENST00000405140.7:c.246+333T>C	ENSP00000385419.3:n.246+333T>C
ENST00000518050.1:n.654T>C
ENST00000519742.5:c.246+333T>C	ENSP00000431026.1:n.246+333T>C
ENST00000520491.5:c.246+333T>C	ENSP00000429881.1:n.246+333T>C
ENST00000520796.5:c.246+333T>C	ENSP00000429336.1:n.246+333T>C
ENST00000522299.5:n.314+333T>C
ENST00000522413.5:c.246+333T>C	ENSP00000428779.1:n.246+333T>C
ENST00000523500.5:c.246+333T>C	ENSP00000429620.1:n.246+333T>C
ENST00000523589.5:c.246+333T>C	ENSP00000431070.1:n.246+333T>C
ENST00000560566.5:c.279+333T>C	ENSP00000453247.1:n.279+333T>C
NM_001831.3:c.246+333T>C	NP_001822.3:n.246+333T>C
NR_038335.1:n.567+333T>C
NR_045494.1:n.426+333T>C
XM_006716284.1:c.402+333T>C	XP_006716347.1:n.402+333T>C
XM_006716284.3:c.402+333T>C	XP_006716347.1:n.402+333T>C
NM_001831.4:c.246+333T>C MANE Select	NP_001822.3:n.246+333T>C
NR_038335.2:n.501+333T>C