Canonical Allele Identifier: CA174275523

Gene: CLU

Linked Data

• dbSNP Id: rs760356108
• gnomAD v2: 8-27466335-GAC-G
• gnomAD v3: 8-27608818-GAC-G
• gnomAD v4: 8-27608818-GAC-G
• MyVariant Identifiers: chr8:g.27466336_27466337del (hg19) ; chr8:g.27608819_27608820del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27608822_27608823del , CM000670.2:g.27608822_27608823del	GRCh38
NC_000008.10:g.27466339_27466340del , CM000670.1:g.27466339_27466340del	GRCh37
NC_000008.9:g.27522256_27522257del	NCBI36
NG_027845.1:g.10991_10992del

Transcript Alleles

HGVS	Amino-acid change
ENST00000316403.15:c.246+118_246+119del MANE Select	ENSP00000315130.10:n.246+118_246+119del
ENST00000316403.14:c.246+118_246+119del	ENSP00000315130.10:n.246+118_246+119del
ENST00000405140.7:c.246+118_246+119del	ENSP00000385419.3:n.246+118_246+119del
ENST00000518050.1:n.439_440del
ENST00000519742.5:c.246+118_246+119del	ENSP00000431026.1:n.246+118_246+119del
ENST00000520491.5:c.246+118_246+119del	ENSP00000429881.1:n.246+118_246+119del
ENST00000520796.5:c.246+118_246+119del	ENSP00000429336.1:n.246+118_246+119del
ENST00000522299.5:n.314+118_314+119del
ENST00000522413.5:c.246+118_246+119del	ENSP00000428779.1:n.246+118_246+119del
ENST00000523500.5:c.246+118_246+119del	ENSP00000429620.1:n.246+118_246+119del
ENST00000523589.5:c.246+118_246+119del	ENSP00000431070.1:n.246+118_246+119del
ENST00000560566.5:c.279+118_279+119del	ENSP00000453247.1:n.279+118_279+119del
NM_001831.3:c.246+118_246+119del	NP_001822.3:n.246+118_246+119del
NR_038335.1:n.567+118_567+119del
NR_045494.1:n.426+118_426+119del
XM_006716284.1:c.402+118_402+119del	XP_006716347.1:n.402+118_402+119del
XM_006716284.3:c.402+118_402+119del	XP_006716347.1:n.402+118_402+119del
NM_001831.4:c.246+118_246+119del MANE Select	NP_001822.3:n.246+118_246+119del
NR_038335.2:n.501+118_501+119del