Canonical Allele Identifier: CA1772891504
Gene: CLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27606997_27606998delinsCA , CM000670.2:g.27606997_27606998delinsCA GRCh38
NC_000008.10:g.27464514_27464515delinsCA , CM000670.1:g.27464514_27464515delinsCA GRCh37
NC_000008.9:g.27520431_27520432delinsCA NCBI36
NG_027845.1:g.12813_12814delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000316403.15:c.247-474_247-473delinsTG MANE Select ENSP00000315130.10:n.247-474_247-473delinsTG
ENST00000316403.14:c.247-474_247-473delinsTG ENSP00000315130.10:n.247-474_247-473delinsTG
ENST00000405140.7:c.247-474_247-473delinsTG ENSP00000385419.3:n.247-474_247-473delinsTG
ENST00000519742.5:c.247-474_247-473delinsTG ENSP00000431026.1:n.247-474_247-473delinsTG
ENST00000520491.5:c.247-474_247-473delinsTG ENSP00000429881.1:n.247-474_247-473delinsTG
ENST00000520796.5:c.247-474_247-473delinsTG ENSP00000429336.1:n.247-474_247-473delinsTG
ENST00000522299.5:n.315-474_315-473delinsTG
ENST00000522413.5:c.247-474_247-473delinsTG ENSP00000428779.1:n.247-474_247-473delinsTG
ENST00000523500.5:c.247-474_247-473delinsTG ENSP00000429620.1:n.247-474_247-473delinsTG
ENST00000523589.5:c.247-474_247-473delinsTG ENSP00000431070.1:n.247-474_247-473delinsTG
ENST00000560566.5:c.280-474_280-473delinsTG ENSP00000453247.1:n.280-474_280-473delinsTG
NM_001831.3:c.247-474_247-473delinsTG NP_001822.3:n.247-474_247-473delinsTG
NR_038335.1:n.568-474_568-473delinsTG
NR_045494.1:n.427-474_427-473delinsTG
XM_006716284.1:c.403-474_403-473delinsTG XP_006716347.1:n.403-474_403-473delinsTG
XM_006716284.3:c.403-474_403-473delinsTG XP_006716347.1:n.403-474_403-473delinsTG
NM_001831.4:c.247-474_247-473delinsTG MANE Select NP_001822.3:n.247-474_247-473delinsTG
NR_038335.2:n.502-474_502-473delinsTG