Canonical Allele Identifier: CA1772894684

Gene: CLU

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27610169C>A , CM000670.2:g.27610169C>A	GRCh38
NC_000008.10:g.27467686C>A , CM000670.1:g.27467686C>A	GRCh37
NC_000008.9:g.27523603C>A	NCBI36
NG_027845.1:g.9642G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316403.15:c.97+306G>T MANE Select	ENSP00000315130.10:n.97+306G>T
ENST00000316403.14:c.97+306G>T	ENSP00000315130.10:n.97+306G>T
ENST00000405140.7:c.97+306G>T	ENSP00000385419.3:n.97+306G>T
ENST00000518050.1:n.172+306G>T
ENST00000519472.5:c.97+306G>T	ENSP00000427868.1:n.97+306G>T
ENST00000519742.5:c.97+306G>T	ENSP00000431026.1:n.97+306G>T
ENST00000520491.5:c.97+306G>T	ENSP00000429881.1:n.97+306G>T
ENST00000520796.5:c.97+306G>T	ENSP00000429336.1:n.97+306G>T
ENST00000522299.5:n.165+306G>T
ENST00000522413.5:c.97+306G>T	ENSP00000428779.1:n.97+306G>T
ENST00000523396.1:c.97+306G>T	ENSP00000428526.1:n.97+306G>T
ENST00000523500.5:c.97+306G>T	ENSP00000429620.1:n.97+306G>T
ENST00000523589.5:c.97+306G>T	ENSP00000431070.1:n.97+306G>T
ENST00000560566.5:c.130+306G>T	ENSP00000453247.1:n.130+306G>T
NM_001831.3:c.97+306G>T	NP_001822.3:n.97+306G>T
NR_038335.1:n.418+306G>T
NR_045494.1:n.277+306G>T
XM_006716284.1:c.253+306G>T	XP_006716347.1:n.253+306G>T
XM_006716284.3:c.253+306G>T	XP_006716347.1:n.253+306G>T
NM_001831.4:c.97+306G>T MANE Select	NP_001822.3:n.97+306G>T
NR_038335.2:n.352+306G>T