Canonical Allele Identifier: CA1167228747
Gene: LRP8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53246956A= , CM000663.2:g.53246956A= GRCh38
NC_000001.10:g.53712628A= , CM000663.1:g.53712628A= GRCh37
NC_000001.9:g.53485216A= NCBI36
NG_011517.2:g.86194T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306052.12:c.*62T= MANE Select ENSP00000303634.6:n.*62T=
ENST00000465675.6:c.2588T= ENSP00000437009.2:n.2588T=
ENST00000480045.6:c.*1119T= ENSP00000433554.2:n.*1119T=
ENST00000529670.6:c.492T=
ENST00000653217.1:c.2489T= ENSP00000499777.1:n.2489T=
ENST00000653810.1:c.1675T=
ENST00000654834.1:n.2414T=
ENST00000654947.1:c.456T= ENSP00000499442.1:n.456T=
ENST00000656486.1:c.2084T= ENSP00000499708.1:n.2084T=
ENST00000657047.1:c.798T=
ENST00000657895.1:c.*62T= ENSP00000499764.1:n.*62T=
ENST00000658277.1:c.*62T= ENSP00000499550.1:n.*62T=
ENST00000658404.1:n.2282T=
ENST00000661457.1:c.*2173T= ENSP00000499547.1:n.*2173T=
ENST00000662198.1:c.*62T= ENSP00000499355.1:n.*62T=
ENST00000662604.1:c.*62T= ENSP00000499486.1:n.*62T=
ENST00000662802.1:c.716T=
ENST00000667377.1:c.2677-975T= ENSP00000499405.1:n.2677-975T=
ENST00000668071.1:c.2361T=
ENST00000668448.1:c.*62T= ENSP00000499273.1:n.*62T=
ENST00000668991.1:n.2667T=
ENST00000669432.1:n.9418T=
ENST00000306052.10:c.*62T= ENSP00000303634.6:n.*62T=
ENST00000354412.7:c.2165T= ENSP00000346391.3:n.2165T=
ENST00000371454.6:c.*62T= ENSP00000360509.2:n.*62T=
ENST00000465675.5:c.*62T= ENSP00000437009.1:n.*62T=
ENST00000529670.5:c.427T=
ENST00000613948.4:c.2162T= ENSP00000480025.1:n.2162T=
NM_001018054.2:c.*62T= NP_001018064.1:n.*62T=
NM_004631.4:c.*62T= NP_004622.2:n.*62T=
NM_017522.4:c.*62T= NP_059992.3:n.*62T=
NM_033300.3:c.*62T= NP_150643.2:n.*62T=
XM_005271173.2:c.*62T= XP_005271230.1:n.*62T=
XM_005271174.2:c.*62T= XP_005271231.1:n.*62T=
XM_005271175.2:c.*62T= XP_005271232.1:n.*62T=
XM_006710881.2:c.*62T= XP_006710944.1:n.*62T=
XM_006710882.2:c.*62T= XP_006710945.1:n.*62T=
XM_011542094.1:c.*62T= XP_011540396.1:n.*62T=
XM_011542095.1:c.*62T= XP_011540397.1:n.*62T=
XM_011542097.1:c.*62T= XP_011540399.1:n.*62T=
XM_005271173.4:c.*62T= XP_005271230.1:n.*62T=
XM_005271174.3:c.*62T= XP_005271231.1:n.*62T=
XM_005271175.3:c.*62T= XP_005271232.1:n.*62T=
XM_006710881.4:c.*62T= XP_006710944.1:n.*62T=
XM_006710882.4:c.*62T= XP_006710945.1:n.*62T=
XM_011542094.2:c.*62T= XP_011540396.1:n.*62T=
XM_011542095.2:c.*62T= XP_011540397.1:n.*62T=
XM_017002265.1:c.*62T= XP_016857754.1:n.*62T=
XM_017002266.2:c.*62T= XP_016857755.1:n.*62T=
XM_017002267.1:c.*62T= XP_016857756.1:n.*62T=
XM_017002268.1:c.*62T= XP_016857757.1:n.*62T=
NM_001018054.3:c.*62T= NP_001018064.1:n.*62T=
NM_004631.5:c.*62T= MANE Select NP_004622.2:n.*62T=
NM_017522.5:c.*62T= NP_059992.3:n.*62T=
NM_033300.4:c.*62T= NP_150643.2:n.*62T=