Canonical Allele Identifier: CA340399627

Gene: LRP8

Linked Data

• dbSNP Id: rs5174
• MyVariant Identifiers: chr1:g.53712727C>G (hg19) ; chr1:g.53247055C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53247055C>G , CM000663.2:g.53247055C>G	GRCh38
NC_000001.10:g.53712727C>G , CM000663.1:g.53712727C>G	GRCh37
NC_000001.9:g.53485315C>G	NCBI36
NG_011517.2:g.86095G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000306052.12:c.2855G>C MANE Select	ENSP00000303634.6:p.Arg952Pro
ENST00000347547.7:c.2345G>C	ENSP00000334522.2:p.Arg782Pro
ENST00000465675.6:c.2489G>C	ENSP00000437009.2:p.Arg830Pro
ENST00000480045.6:c.*1020G>C	ENSP00000433554.2:n.*1020G>C
ENST00000529670.6:c.393G>C
ENST00000653217.1:c.2390G>C	ENSP00000499777.1:p.Arg797Pro
ENST00000653810.1:c.1576G>C
ENST00000654834.1:n.2315G>C
ENST00000654947.1:c.357G>C	ENSP00000499442.1:p.Ala119=
ENST00000656486.1:c.1985G>C	ENSP00000499708.1:p.Arg662Pro
ENST00000657047.1:c.699G>C
ENST00000657895.1:c.2336G>C	ENSP00000499764.1:p.Arg779Pro
ENST00000658277.1:c.2090G>C	ENSP00000499550.1:p.Arg697Pro
ENST00000658404.1:n.2183G>C
ENST00000661457.1:c.*2074G>C	ENSP00000499547.1:n.*2074G>C
ENST00000662198.1:c.2468G>C	ENSP00000499355.1:p.Arg823Pro
ENST00000662604.1:c.2162G>C	ENSP00000499486.1:p.Arg721Pro
ENST00000662802.1:c.617G>C
ENST00000667377.1:c.2677-1074G>C	ENSP00000499405.1:n.2677-1074G>C
ENST00000668071.1:c.2262G>C
ENST00000668448.1:c.2630G>C	ENSP00000499273.1:p.Arg877Pro
ENST00000668991.1:n.2568G>C
ENST00000669432.1:n.9319G>C
ENST00000306052.10:c.2855G>C	ENSP00000303634.6:p.Arg952Pro
ENST00000347547.6:c.2345G>C	ENSP00000334522.2:p.Arg782Pro
ENST00000354412.7:c.2066G>C	ENSP00000346391.3:p.Arg689Pro
ENST00000371454.6:c.2678G>C	ENSP00000360509.2:p.Arg893Pro
ENST00000465675.5:c.1337G>C	ENSP00000437009.1:p.Arg446Pro
ENST00000480045.5:c.*1797G>C	ENSP00000433554.1:n.*1797G>C
ENST00000529670.5:c.328G>C
ENST00000613948.4:c.2063G>C	ENSP00000480025.1:p.Arg688Pro
NM_001018054.2:c.2678G>C	NP_001018064.1:p.Arg893Pro
NM_004631.4:c.2855G>C	NP_004622.2:p.Arg952Pro
NM_017522.4:c.2066G>C	NP_059992.3:p.Arg689Pro
NM_033300.3:c.2345G>C	NP_150643.2:p.Arg782Pro
XM_005271173.2:c.2894G>C	XP_005271230.1:p.Arg965Pro
XM_005271174.2:c.2507G>C	XP_005271231.1:p.Arg836Pro
XM_005271175.2:c.2468G>C	XP_005271232.1:p.Arg823Pro
XM_006710881.2:c.2717G>C	XP_006710944.1:p.Arg906Pro
XM_006710882.2:c.2669G>C	XP_006710945.1:p.Arg890Pro
XM_011542094.1:c.2768G>C	XP_011540396.1:p.Arg923Pro
XM_011542095.1:c.2378G>C	XP_011540397.1:p.Arg793Pro
XM_011542097.1:c.2981G>C	XP_011540399.1:p.Arg994Pro
XM_005271173.4:c.2894G>C	XP_005271230.1:p.Arg965Pro
XM_005271174.3:c.2507G>C	XP_005271231.1:p.Arg836Pro
XM_005271175.3:c.2468G>C	XP_005271232.1:p.Arg823Pro
XM_006710881.4:c.2717G>C	XP_006710944.1:p.Arg906Pro
XM_006710882.4:c.2669G>C	XP_006710945.1:p.Arg890Pro
XM_011542094.2:c.2768G>C	XP_011540396.1:p.Arg923Pro
XM_011542095.2:c.2378G>C	XP_011540397.1:p.Arg793Pro
XM_017002265.1:c.2729G>C	XP_016857754.1:p.Arg910Pro
XM_017002266.2:c.2492G>C	XP_016857755.1:p.Arg831Pro
XM_017002267.1:c.1637G>C	XP_016857756.1:p.Arg546Pro
XM_017002268.1:c.1637G>C	XP_016857757.1:p.Arg546Pro
NM_001018054.3:c.2678G>C	NP_001018064.1:p.Arg893Pro
NM_004631.5:c.2855G>C MANE Select	NP_004622.2:p.Arg952Pro
NM_017522.5:c.2066G>C	NP_059992.3:p.Arg689Pro
NM_033300.4:c.2345G>C	NP_150643.2:p.Arg782Pro