Canonical Allele Identifier: CA4691060

Gene: CLU

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27609061G>A , CM000670.2:g.27609061G>A	GRCh38
NC_000008.10:g.27466578G>A , CM000670.1:g.27466578G>A	GRCh37
NC_000008.9:g.27522495G>A	NCBI36
NG_027845.1:g.10750C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001831.4:c.123C>T MANE Select	NP_001822.3:p.Tyr41=
ENST00000316403.15:c.123C>T MANE Select	ENSP00000315130.10:p.Tyr41=
NM_001831.3:c.123C>T	NP_001822.3:p.Tyr41=
NR_038335.1:n.444C>T
NR_038335.2:n.378C>T
NR_045494.1:n.303C>T
ENST00000316403.14:c.123C>T	ENSP00000315130.10:p.Tyr41=
ENST00000405140.7:c.123C>T	ENSP00000385419.3:p.Tyr41=
ENST00000518050.1:n.198C>T
ENST00000519472.5:c.123C>T	ENSP00000427868.1:p.Tyr41=
ENST00000519742.5:c.123C>T	ENSP00000431026.1:p.Tyr41=
ENST00000520491.5:c.123C>T	ENSP00000429881.1:p.Tyr41=
ENST00000520796.5:c.123C>T	ENSP00000429336.1:p.Tyr41=
ENST00000522299.5:n.191C>T
ENST00000522413.5:c.123C>T	ENSP00000428779.1:p.Tyr41=
ENST00000523396.1:c.123C>T	ENSP00000428526.1:p.Tyr41=
ENST00000523500.5:c.123C>T	ENSP00000429620.1:p.Tyr41=
ENST00000523589.5:c.123C>T	ENSP00000431070.1:p.Tyr41=
ENST00000560566.5:c.156C>T	ENSP00000453247.1:p.Tyr52=
XM_006716284.1:c.279C>T	XP_006716347.1:p.Tyr93=
XM_006716284.3:c.279C>T	XP_006716347.1:p.Tyr93=