Canonical Allele Identifier: CA1772927366
Gene: CLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27598736T>G , CM000670.2:g.27598736T>G GRCh38
NC_000008.10:g.27456253T>G , CM000670.1:g.27456253T>G GRCh37
NC_000008.9:g.27512170T>G NCBI36
NG_027845.1:g.21075A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000316403.15:c.1165-101A>C MANE Select ENSP00000315130.10:n.1165-101A>C
ENST00000316403.14:c.1165-101A>C ENSP00000315130.10:n.1165-101A>C
ENST00000405140.7:c.1165-101A>C ENSP00000385419.3:n.1165-101A>C
ENST00000521770.1:c.237-101A>C
ENST00000522098.1:c.752-101A>C
ENST00000522299.5:n.2276A>C
ENST00000523500.5:c.1165-101A>C ENSP00000429620.1:n.1165-101A>C
NM_001831.3:c.1165-101A>C NP_001822.3:n.1165-101A>C
NR_038335.1:n.1486-101A>C
NR_045494.1:n.1345-101A>C
XM_006716284.1:c.1321-101A>C XP_006716347.1:n.1321-101A>C
XM_006716284.3:c.1321-101A>C XP_006716347.1:n.1321-101A>C
NM_001831.4:c.1165-101A>C MANE Select NP_001822.3:n.1165-101A>C
NR_038335.2:n.1420-101A>C