Canonical Allele Identifier: CA1772893369
Gene: CLU HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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