Canonical Allele Identifier: CA1772893371
Gene: CLU HGNC NCBI

Linked Data

dbSNP Id: rs1800868414

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27608818G>A , CM000670.2:g.27608818G>A GRCh38
NC_000008.10:g.27466335G>A , CM000670.1:g.27466335G>A GRCh37
NC_000008.9:g.27522252G>A NCBI36
NG_027845.1:g.10993C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000316403.15:c.246+120C>T MANE Select ENSP00000315130.10:n.246+120C>T
ENST00000316403.14:c.246+120C>T ENSP00000315130.10:n.246+120C>T
ENST00000405140.7:c.246+120C>T ENSP00000385419.3:n.246+120C>T
ENST00000518050.1:n.441C>T
ENST00000519742.5:c.246+120C>T ENSP00000431026.1:n.246+120C>T
ENST00000520491.5:c.246+120C>T ENSP00000429881.1:n.246+120C>T
ENST00000520796.5:c.246+120C>T ENSP00000429336.1:n.246+120C>T
ENST00000522299.5:n.314+120C>T
ENST00000522413.5:c.246+120C>T ENSP00000428779.1:n.246+120C>T
ENST00000523500.5:c.246+120C>T ENSP00000429620.1:n.246+120C>T
ENST00000523589.5:c.246+120C>T ENSP00000431070.1:n.246+120C>T
ENST00000560566.5:c.279+120C>T ENSP00000453247.1:n.279+120C>T
NM_001831.3:c.246+120C>T NP_001822.3:n.246+120C>T
NR_038335.1:n.567+120C>T
NR_045494.1:n.426+120C>T
XM_006716284.1:c.402+120C>T XP_006716347.1:n.402+120C>T
XM_006716284.3:c.402+120C>T XP_006716347.1:n.402+120C>T
NM_001831.4:c.246+120C>T MANE Select NP_001822.3:n.246+120C>T
NR_038335.2:n.501+120C>T