Canonical Allele Identifier: CA10838043

Gene: LRP8

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53311959A>C , CM000663.2:g.53311959A>C	GRCh38
NC_000001.10:g.53777631A>C , CM000663.1:g.53777631A>C	GRCh37
NC_000001.9:g.53550219A>C	NCBI36
NG_011517.2:g.21191T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306052.12:c.244+14914T>G MANE Select	ENSP00000303634.6:n.244+14914T>G
ENST00000347547.7:c.244+14914T>G	ENSP00000334522.2:n.244+14914T>G
ENST00000465675.6:c.226+14914T>G	ENSP00000437009.2:n.226+14914T>G
ENST00000480045.6:c.244+14914T>G	ENSP00000433554.2:n.244+14914T>G
ENST00000654634.1:n.395+14914T>G
ENST00000655704.1:n.326+14914T>G
ENST00000657895.1:c.244+14914T>G	ENSP00000499764.1:n.244+14914T>G
ENST00000658277.1:c.244+14914T>G	ENSP00000499550.1:n.244+14914T>G
ENST00000658404.1:n.262+14914T>G
ENST00000659993.1:c.244+14914T>G	ENSP00000499697.1:n.244+14914T>G
ENST00000661359.1:n.382+14914T>G
ENST00000661457.1:c.*329+1010T>G	ENSP00000499547.1:n.*329+1010T>G
ENST00000662198.1:c.244+14914T>G	ENSP00000499355.1:n.244+14914T>G
ENST00000662604.1:c.244+14914T>G	ENSP00000499486.1:n.244+14914T>G
ENST00000667377.1:c.244+14914T>G	ENSP00000499405.1:n.244+14914T>G
ENST00000668071.1:c.215+14914T>G
ENST00000668448.1:c.244+14914T>G	ENSP00000499273.1:n.244+14914T>G
ENST00000668991.1:n.305+14914T>G
ENST00000669432.1:n.370+14914T>G
ENST00000306052.10:c.244+14914T>G	ENSP00000303634.6:n.244+14914T>G
ENST00000347547.6:c.244+14914T>G	ENSP00000334522.2:n.244+14914T>G
ENST00000354412.7:c.244+14914T>G	ENSP00000346391.3:n.244+14914T>G
ENST00000371454.6:c.244+14914T>G	ENSP00000360509.2:n.244+14914T>G
ENST00000465675.5:c.-585+14914T>G	ENSP00000437009.1:n.-585+14914T>G
ENST00000480045.5:c.244+14914T>G	ENSP00000433554.1:n.244+14914T>G
ENST00000496580.1:n.149+14914T>G
ENST00000613948.4:c.244+14914T>G	ENSP00000480025.1:n.244+14914T>G
NM_001018054.2:c.244+14914T>G	NP_001018064.1:n.244+14914T>G
NM_004631.4:c.244+14914T>G	NP_004622.2:n.244+14914T>G
NM_017522.4:c.244+14914T>G	NP_059992.3:n.244+14914T>G
NM_033300.3:c.244+14914T>G	NP_150643.2:n.244+14914T>G
XM_005271173.2:c.244+14914T>G	XP_005271230.1:n.244+14914T>G
XM_005271174.2:c.244+14914T>G	XP_005271231.1:n.244+14914T>G
XM_005271175.2:c.244+14914T>G	XP_005271232.1:n.244+14914T>G
XM_006710881.2:c.244+14914T>G	XP_006710944.1:n.244+14914T>G
XM_006710882.2:c.244+14914T>G	XP_006710945.1:n.244+14914T>G
XM_011542094.1:c.244+14914T>G	XP_011540396.1:n.244+14914T>G
XM_011542095.1:c.244+14914T>G	XP_011540397.1:n.244+14914T>G
XM_011542096.1:c.244+14914T>G	XP_011540398.1:n.244+14914T>G
XM_011542097.1:c.244+14914T>G	XP_011540399.1:n.244+14914T>G
XM_005271173.4:c.244+14914T>G	XP_005271230.1:n.244+14914T>G
XM_005271174.3:c.244+14914T>G	XP_005271231.1:n.244+14914T>G
XM_005271175.3:c.244+14914T>G	XP_005271232.1:n.244+14914T>G
XM_006710881.4:c.244+14914T>G	XP_006710944.1:n.244+14914T>G
XM_006710882.4:c.244+14914T>G	XP_006710945.1:n.244+14914T>G
XM_011542094.2:c.244+14914T>G	XP_011540396.1:n.244+14914T>G
XM_011542095.2:c.244+14914T>G	XP_011540397.1:n.244+14914T>G
XM_011542096.2:c.244+14914T>G	XP_011540398.1:n.244+14914T>G
XM_017002265.1:c.244+14914T>G	XP_016857754.1:n.244+14914T>G
XM_017002266.2:c.244+14914T>G	XP_016857755.1:n.244+14914T>G
XM_017002267.1:c.-588+14914T>G	XP_016857756.1:n.-588+14914T>G
XM_017002268.1:c.-627+14914T>G	XP_016857757.1:n.-627+14914T>G
XR_002958307.1:n.17948A>C
NM_001018054.3:c.244+14914T>G	NP_001018064.1:n.244+14914T>G
NM_004631.5:c.244+14914T>G MANE Select	NP_004622.2:n.244+14914T>G
NM_017522.5:c.244+14914T>G	NP_059992.3:n.244+14914T>G
NM_033300.4:c.244+14914T>G	NP_150643.2:n.244+14914T>G