Canonical Allele Identifier: CA340399509

Gene: LRP8

Linked Data

• dbSNP Id: rs773281713
• MyVariant Identifiers: chr1:g.53712702A>T (hg19) ; chr1:g.53247030A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53247030A>T , CM000663.2:g.53247030A>T	GRCh38
NC_000001.10:g.53712702A>T , CM000663.1:g.53712702A>T	GRCh37
NC_000001.9:g.53485290A>T	NCBI36
NG_011517.2:g.86120T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306052.12:c.2880T>A MANE Select	ENSP00000303634.6:p.Asp960Glu
ENST00000347547.7:c.2370T>A	ENSP00000334522.2:p.Asp790Glu
ENST00000465675.6:c.2514T>A	ENSP00000437009.2:p.Asp838Glu
ENST00000480045.6:c.*1045T>A	ENSP00000433554.2:n.*1045T>A
ENST00000529670.6:c.418T>A
ENST00000653217.1:c.2415T>A	ENSP00000499777.1:p.Asp805Glu
ENST00000653810.1:c.1601T>A
ENST00000654834.1:n.2340T>A
ENST00000654947.1:c.382T>A	ENSP00000499442.1:n.382T>A
ENST00000656486.1:c.2010T>A	ENSP00000499708.1:p.Asp670Glu
ENST00000657047.1:c.724T>A
ENST00000657895.1:c.2361T>A	ENSP00000499764.1:p.Asp787Glu
ENST00000658277.1:c.2115T>A	ENSP00000499550.1:p.Asp705Glu
ENST00000658404.1:n.2208T>A
ENST00000661457.1:c.*2099T>A	ENSP00000499547.1:n.*2099T>A
ENST00000662198.1:c.2493T>A	ENSP00000499355.1:p.Asp831Glu
ENST00000662604.1:c.2187T>A	ENSP00000499486.1:p.Asp729Glu
ENST00000662802.1:c.642T>A
ENST00000667377.1:c.2677-1049T>A	ENSP00000499405.1:n.2677-1049T>A
ENST00000668071.1:c.2287T>A
ENST00000668448.1:c.2655T>A	ENSP00000499273.1:p.Asp885Glu
ENST00000668991.1:n.2593T>A
ENST00000669432.1:n.9344T>A
ENST00000306052.10:c.2880T>A	ENSP00000303634.6:p.Asp960Glu
ENST00000347547.6:c.2370T>A	ENSP00000334522.2:p.Asp790Glu
ENST00000354412.7:c.2091T>A	ENSP00000346391.3:p.Asp697Glu
ENST00000371454.6:c.2703T>A	ENSP00000360509.2:p.Asp901Glu
ENST00000465675.5:c.1362T>A	ENSP00000437009.1:p.Asp454Glu
ENST00000480045.5:c.*1822T>A	ENSP00000433554.1:n.*1822T>A
ENST00000529670.5:c.353T>A
ENST00000613948.4:c.2088T>A	ENSP00000480025.1:p.Asp696Glu
NM_001018054.2:c.2703T>A	NP_001018064.1:p.Asp901Glu
NM_004631.4:c.2880T>A	NP_004622.2:p.Asp960Glu
NM_017522.4:c.2091T>A	NP_059992.3:p.Asp697Glu
NM_033300.3:c.2370T>A	NP_150643.2:p.Asp790Glu
XM_005271173.2:c.2919T>A	XP_005271230.1:p.Asp973Glu
XM_005271174.2:c.2532T>A	XP_005271231.1:p.Asp844Glu
XM_005271175.2:c.2493T>A	XP_005271232.1:p.Asp831Glu
XM_006710881.2:c.2742T>A	XP_006710944.1:p.Asp914Glu
XM_006710882.2:c.2694T>A	XP_006710945.1:p.Asp898Glu
XM_011542094.1:c.2793T>A	XP_011540396.1:p.Asp931Glu
XM_011542095.1:c.2403T>A	XP_011540397.1:p.Asp801Glu
XM_011542097.1:c.3006T>A	XP_011540399.1:p.Asp1002Glu
XM_005271173.4:c.2919T>A	XP_005271230.1:p.Asp973Glu
XM_005271174.3:c.2532T>A	XP_005271231.1:p.Asp844Glu
XM_005271175.3:c.2493T>A	XP_005271232.1:p.Asp831Glu
XM_006710881.4:c.2742T>A	XP_006710944.1:p.Asp914Glu
XM_006710882.4:c.2694T>A	XP_006710945.1:p.Asp898Glu
XM_011542094.2:c.2793T>A	XP_011540396.1:p.Asp931Glu
XM_011542095.2:c.2403T>A	XP_011540397.1:p.Asp801Glu
XM_017002265.1:c.2754T>A	XP_016857754.1:p.Asp918Glu
XM_017002266.2:c.2517T>A	XP_016857755.1:p.Asp839Glu
XM_017002267.1:c.1662T>A	XP_016857756.1:p.Asp554Glu
XM_017002268.1:c.1662T>A	XP_016857757.1:p.Asp554Glu
NM_001018054.3:c.2703T>A	NP_001018064.1:p.Asp901Glu
NM_004631.5:c.2880T>A MANE Select	NP_004622.2:p.Asp960Glu
NM_017522.5:c.2091T>A	NP_059992.3:p.Asp697Glu
NM_033300.4:c.2370T>A	NP_150643.2:p.Asp790Glu