Canonical Allele Identifier: CA10725511

Gene: LRP8

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53246063G>C , CM000663.2:g.53246063G>C	GRCh38
NC_000001.10:g.53711735G>C , CM000663.1:g.53711735G>C	GRCh37
NC_000001.9:g.53484323G>C	NCBI36
NG_011517.2:g.87087C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306052.12:c.*955C>G MANE Select	ENSP00000303634.6:n.*955C>G
ENST00000480045.6:c.*2012C>G	ENSP00000433554.2:n.*2012C>G
ENST00000529670.6:c.525-82C>G
ENST00000653217.1:c.3382C>G	ENSP00000499777.1:n.3382C>G
ENST00000653810.1:c.1676-82C>G
ENST00000654834.1:n.3307C>G
ENST00000657047.1:c.837-82C>G
ENST00000657895.1:c.*955C>G	ENSP00000499764.1:n.*955C>G
ENST00000658277.1:c.*955C>G	ENSP00000499550.1:n.*955C>G
ENST00000661457.1:c.*3066C>G	ENSP00000499547.1:n.*3066C>G
ENST00000662198.1:c.*955C>G	ENSP00000499355.1:n.*955C>G
ENST00000667377.1:c.2677-82C>G	ENSP00000499405.1:n.2677-82C>G
ENST00000668071.1:c.3254C>G
ENST00000668448.1:c.*955C>G	ENSP00000499273.1:n.*955C>G
ENST00000669432.1:n.10311C>G
ENST00000306052.10:c.*955C>G	ENSP00000303634.6:n.*955C>G
ENST00000529670.5:c.428-82C>G
NM_001018054.2:c.*955C>G	NP_001018064.1:n.*955C>G
NM_004631.4:c.*955C>G	NP_004622.2:n.*955C>G
NM_017522.4:c.*955C>G	NP_059992.3:n.*955C>G
NM_033300.3:c.*955C>G	NP_150643.2:n.*955C>G
XM_005271173.2:c.*955C>G	XP_005271230.1:n.*955C>G
XM_005271174.2:c.*955C>G	XP_005271231.1:n.*955C>G
XM_005271175.2:c.*955C>G	XP_005271232.1:n.*955C>G
XM_006710881.2:c.*955C>G	XP_006710944.1:n.*955C>G
XM_006710882.2:c.*955C>G	XP_006710945.1:n.*955C>G
XM_011542094.1:c.*955C>G	XP_011540396.1:n.*955C>G
XM_011542095.1:c.*955C>G	XP_011540397.1:n.*955C>G
XM_011542097.1:c.*955C>G	XP_011540399.1:n.*955C>G
XM_005271173.4:c.*955C>G	XP_005271230.1:n.*955C>G
XM_005271174.3:c.*955C>G	XP_005271231.1:n.*955C>G
XM_005271175.3:c.*955C>G	XP_005271232.1:n.*955C>G
XM_006710881.4:c.*955C>G	XP_006710944.1:n.*955C>G
XM_006710882.4:c.*955C>G	XP_006710945.1:n.*955C>G
XM_011542094.2:c.*955C>G	XP_011540396.1:n.*955C>G
XM_011542095.2:c.*955C>G	XP_011540397.1:n.*955C>G
XM_017002265.1:c.*955C>G	XP_016857754.1:n.*955C>G
XM_017002266.2:c.*955C>G	XP_016857755.1:n.*955C>G
XM_017002267.1:c.*955C>G	XP_016857756.1:n.*955C>G
XM_017002268.1:c.*955C>G	XP_016857757.1:n.*955C>G
NM_001018054.3:c.*955C>G	NP_001018064.1:n.*955C>G
NM_004631.5:c.*955C>G MANE Select	NP_004622.2:n.*955C>G
NM_017522.5:c.*955C>G	NP_059992.3:n.*955C>G
NM_033300.4:c.*955C>G	NP_150643.2:n.*955C>G