Canonical Allele Identifier: CA1167228759
Gene: LRP8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53246980A= , CM000663.2:g.53246980A= GRCh38
NC_000001.10:g.53712652A= , CM000663.1:g.53712652A= GRCh37
NC_000001.9:g.53485240A= NCBI36
NG_011517.2:g.86170T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306052.12:c.*38T= MANE Select ENSP00000303634.6:n.*38T=
ENST00000465675.6:c.2564T= ENSP00000437009.2:n.2564T=
ENST00000480045.6:c.*1095T= ENSP00000433554.2:n.*1095T=
ENST00000529670.6:c.468T=
ENST00000653217.1:c.2465T= ENSP00000499777.1:n.2465T=
ENST00000653810.1:c.1651T=
ENST00000654834.1:n.2390T=
ENST00000654947.1:c.432T= ENSP00000499442.1:n.432T=
ENST00000656486.1:c.2060T= ENSP00000499708.1:n.2060T=
ENST00000657047.1:c.774T=
ENST00000657895.1:c.*38T= ENSP00000499764.1:n.*38T=
ENST00000658277.1:c.*38T= ENSP00000499550.1:n.*38T=
ENST00000658404.1:n.2258T=
ENST00000661457.1:c.*2149T= ENSP00000499547.1:n.*2149T=
ENST00000662198.1:c.*38T= ENSP00000499355.1:n.*38T=
ENST00000662604.1:c.*38T= ENSP00000499486.1:n.*38T=
ENST00000662802.1:c.692T=
ENST00000667377.1:c.2677-999T= ENSP00000499405.1:n.2677-999T=
ENST00000668071.1:c.2337T=
ENST00000668448.1:c.*38T= ENSP00000499273.1:n.*38T=
ENST00000668991.1:n.2643T=
ENST00000669432.1:n.9394T=
ENST00000306052.10:c.*38T= ENSP00000303634.6:n.*38T=
ENST00000354412.7:c.2141T= ENSP00000346391.3:n.2141T=
ENST00000371454.6:c.*38T= ENSP00000360509.2:n.*38T=
ENST00000465675.5:c.*38T= ENSP00000437009.1:n.*38T=
ENST00000480045.5:c.*1872T= ENSP00000433554.1:n.*1872T=
ENST00000529670.5:c.403T=
ENST00000613948.4:c.2138T= ENSP00000480025.1:n.2138T=
NM_001018054.2:c.*38T= NP_001018064.1:n.*38T=
NM_004631.4:c.*38T= NP_004622.2:n.*38T=
NM_017522.4:c.*38T= NP_059992.3:n.*38T=
NM_033300.3:c.*38T= NP_150643.2:n.*38T=
XM_005271173.2:c.*38T= XP_005271230.1:n.*38T=
XM_005271174.2:c.*38T= XP_005271231.1:n.*38T=
XM_005271175.2:c.*38T= XP_005271232.1:n.*38T=
XM_006710881.2:c.*38T= XP_006710944.1:n.*38T=
XM_006710882.2:c.*38T= XP_006710945.1:n.*38T=
XM_011542094.1:c.*38T= XP_011540396.1:n.*38T=
XM_011542095.1:c.*38T= XP_011540397.1:n.*38T=
XM_011542097.1:c.*38T= XP_011540399.1:n.*38T=
XM_005271173.4:c.*38T= XP_005271230.1:n.*38T=
XM_005271174.3:c.*38T= XP_005271231.1:n.*38T=
XM_005271175.3:c.*38T= XP_005271232.1:n.*38T=
XM_006710881.4:c.*38T= XP_006710944.1:n.*38T=
XM_006710882.4:c.*38T= XP_006710945.1:n.*38T=
XM_011542094.2:c.*38T= XP_011540396.1:n.*38T=
XM_011542095.2:c.*38T= XP_011540397.1:n.*38T=
XM_017002265.1:c.*38T= XP_016857754.1:n.*38T=
XM_017002266.2:c.*38T= XP_016857755.1:n.*38T=
XM_017002267.1:c.*38T= XP_016857756.1:n.*38T=
XM_017002268.1:c.*38T= XP_016857757.1:n.*38T=
NM_001018054.3:c.*38T= NP_001018064.1:n.*38T=
NM_004631.5:c.*38T= MANE Select NP_004622.2:n.*38T=
NM_017522.5:c.*38T= NP_059992.3:n.*38T=
NM_033300.4:c.*38T= NP_150643.2:n.*38T=