Canonical Allele Identifier: CA1772893356

Gene: CLU

Linked Data

• dbSNP Id: rs1800868147

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27608803del , CM000670.2:g.27608803del	GRCh38
NC_000008.10:g.27466320del , CM000670.1:g.27466320del	GRCh37
NC_000008.9:g.27522237del	NCBI36
NG_027845.1:g.11008del

Transcript Alleles

HGVS	Amino-acid change
ENST00000316403.15:c.246+135del MANE Select	ENSP00000315130.10:n.246+135del
ENST00000316403.14:c.246+135del	ENSP00000315130.10:n.246+135del
ENST00000405140.7:c.246+135del	ENSP00000385419.3:n.246+135del
ENST00000518050.1:n.456del
ENST00000519742.5:c.246+135del	ENSP00000431026.1:n.246+135del
ENST00000520491.5:c.246+135del	ENSP00000429881.1:n.246+135del
ENST00000520796.5:c.246+135del	ENSP00000429336.1:n.246+135del
ENST00000522299.5:n.314+135del
ENST00000522413.5:c.246+135del	ENSP00000428779.1:n.246+135del
ENST00000523500.5:c.246+135del	ENSP00000429620.1:n.246+135del
ENST00000523589.5:c.246+135del	ENSP00000431070.1:n.246+135del
ENST00000560566.5:c.279+135del	ENSP00000453247.1:n.279+135del
NM_001831.3:c.246+135del	NP_001822.3:n.246+135del
NR_038335.1:n.567+135del
NR_045494.1:n.426+135del
XM_006716284.1:c.402+135del	XP_006716347.1:n.402+135del
XM_006716284.3:c.402+135del	XP_006716347.1:n.402+135del
NM_001831.4:c.246+135del MANE Select	NP_001822.3:n.246+135del
NR_038335.2:n.501+135del