Canonical Allele Identifier: CA1144212696
Gene: LRP8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53246998C= , CM000663.2:g.53246998C= GRCh38
NC_000001.10:g.53712670C= , CM000663.1:g.53712670C= GRCh37
NC_000001.9:g.53485258C= NCBI36
NG_011517.2:g.86152G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306052.12:c.*20G= MANE Select ENSP00000303634.6:n.*20G=
ENST00000465675.6:c.2546G= ENSP00000437009.2:n.2546G=
ENST00000480045.6:c.*1077G= ENSP00000433554.2:n.*1077G=
ENST00000529670.6:c.450G=
ENST00000653217.1:c.2447G= ENSP00000499777.1:n.2447G=
ENST00000653810.1:c.1633G=
ENST00000654834.1:n.2372G=
ENST00000654947.1:c.414G= ENSP00000499442.1:n.414G=
ENST00000656486.1:c.2042G= ENSP00000499708.1:n.2042G=
ENST00000657047.1:c.756G=
ENST00000657895.1:c.*20G= ENSP00000499764.1:n.*20G=
ENST00000658277.1:c.*20G= ENSP00000499550.1:n.*20G=
ENST00000658404.1:n.2240G=
ENST00000661457.1:c.*2131G= ENSP00000499547.1:n.*2131G=
ENST00000662198.1:c.*20G= ENSP00000499355.1:n.*20G=
ENST00000662604.1:c.*20G= ENSP00000499486.1:n.*20G=
ENST00000662802.1:c.674G=
ENST00000667377.1:c.2677-1017G= ENSP00000499405.1:n.2677-1017G=
ENST00000668071.1:c.2319G=
ENST00000668448.1:c.*20G= ENSP00000499273.1:n.*20G=
ENST00000668991.1:n.2625G=
ENST00000669432.1:n.9376G=
ENST00000306052.10:c.*20G= ENSP00000303634.6:n.*20G=
ENST00000354412.7:c.2123G= ENSP00000346391.3:n.2123G=
ENST00000371454.6:c.*20G= ENSP00000360509.2:n.*20G=
ENST00000465675.5:c.*20G= ENSP00000437009.1:n.*20G=
ENST00000480045.5:c.*1854G= ENSP00000433554.1:n.*1854G=
ENST00000529670.5:c.385G=
ENST00000613948.4:c.2120G= ENSP00000480025.1:n.2120G=
NM_001018054.2:c.*20G= NP_001018064.1:n.*20G=
NM_004631.4:c.*20G= NP_004622.2:n.*20G=
NM_017522.4:c.*20G= NP_059992.3:n.*20G=
NM_033300.3:c.*20G= NP_150643.2:n.*20G=
XM_005271173.2:c.*20G= XP_005271230.1:n.*20G=
XM_005271174.2:c.*20G= XP_005271231.1:n.*20G=
XM_005271175.2:c.*20G= XP_005271232.1:n.*20G=
XM_006710881.2:c.*20G= XP_006710944.1:n.*20G=
XM_006710882.2:c.*20G= XP_006710945.1:n.*20G=
XM_011542094.1:c.*20G= XP_011540396.1:n.*20G=
XM_011542095.1:c.*20G= XP_011540397.1:n.*20G=
XM_011542097.1:c.*20G= XP_011540399.1:n.*20G=
XM_005271173.4:c.*20G= XP_005271230.1:n.*20G=
XM_005271174.3:c.*20G= XP_005271231.1:n.*20G=
XM_005271175.3:c.*20G= XP_005271232.1:n.*20G=
XM_006710881.4:c.*20G= XP_006710944.1:n.*20G=
XM_006710882.4:c.*20G= XP_006710945.1:n.*20G=
XM_011542094.2:c.*20G= XP_011540396.1:n.*20G=
XM_011542095.2:c.*20G= XP_011540397.1:n.*20G=
XM_017002265.1:c.*20G= XP_016857754.1:n.*20G=
XM_017002266.2:c.*20G= XP_016857755.1:n.*20G=
XM_017002267.1:c.*20G= XP_016857756.1:n.*20G=
XM_017002268.1:c.*20G= XP_016857757.1:n.*20G=
NM_001018054.3:c.*20G= NP_001018064.1:n.*20G=
NM_004631.5:c.*20G= MANE Select NP_004622.2:n.*20G=
NM_017522.5:c.*20G= NP_059992.3:n.*20G=
NM_033300.4:c.*20G= NP_150643.2:n.*20G=