Canonical Allele Identifier: CA2494002747
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43945336G= , CM000664.2:g.43945336G= GRCh38
NC_000002.11:g.44172475G= , CM000664.1:g.44172475G= GRCh37
NC_000002.10:g.44025979G= NCBI36
NG_008247.1:g.55670C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409659.6:c.2292C= ENSP00000386562.2:p.Leu764=
ENST00000447246.2:c.2292C= ENSP00000403637.2:p.Leu764=
ENST00000681961.1:n.2312C=
ENST00000682104.1:c.2166C= ENSP00000507716.1:p.Leu722=
ENST00000682303.1:c.*2082+777C= ENSP00000508325.1:n.*2082+777C=
ENST00000682308.1:c.2292C= ENSP00000507056.1:p.Leu764=
ENST00000682480.1:c.2292C= ENSP00000508344.1:p.Leu764=
ENST00000682546.1:c.2289C= ENSP00000508188.1:p.Leu763=
ENST00000682585.1:c.2292C= ENSP00000506885.1:p.Leu764=
ENST00000682595.1:n.2874C=
ENST00000682607.1:c.710C=
ENST00000682779.1:c.2283C= ENSP00000507947.1:p.Leu761=
ENST00000682885.1:c.2247C= ENSP00000508036.1:p.Leu749=
ENST00000682933.1:n.2366C=
ENST00000683072.1:n.2874C=
ENST00000683125.1:c.2292C= ENSP00000507939.1:p.Leu764=
ENST00000683213.1:c.2295C= ENSP00000507751.1:p.Leu765=
ENST00000683220.1:c.2322C= ENSP00000507151.1:p.Leu774=
ENST00000683329.1:n.3095C=
ENST00000683346.1:c.*2167C= ENSP00000507458.1:n.*2167C=
ENST00000683459.1:n.2879C=
ENST00000683590.1:c.2292C= ENSP00000506820.1:p.Leu764=
ENST00000683623.1:c.2292C= ENSP00000507702.1:p.Leu764=
ENST00000683645.1:n.2843C=
ENST00000683694.1:n.1043C=
ENST00000683796.1:c.*2164C= ENSP00000508221.1:n.*2164C=
ENST00000683802.1:n.5217C=
ENST00000683833.1:c.2283C= ENSP00000506852.1:p.Leu761=
ENST00000683934.1:c.2178C=
ENST00000683989.1:c.2292C= ENSP00000507510.1:p.Leu764=
ENST00000683994.1:c.2292C= ENSP00000507181.1:p.Leu764=
ENST00000684290.1:c.2210+777C= ENSP00000507243.1:n.2210+777C=
ENST00000684306.1:c.*2205C= ENSP00000508384.1:n.*2205C=
ENST00000684341.1:n.2312C=
ENST00000684383.1:c.*1930C= ENSP00000506863.1:n.*1930C=
ENST00000684619.1:c.*2164C= ENSP00000508088.1:n.*2164C=
ENST00000684743.1:n.3323C=
ENST00000260665.12:c.2292C= MANE Select ENSP00000260665.7:p.Leu764=
ENST00000260665.11:c.2292C= ENSP00000260665.7:p.Leu764=
NM_133259.3:c.2292C= NP_573566.2:p.Leu764=
XM_006711915.2:c.2214C= XP_006711978.1:p.Leu738=
XM_006711916.2:c.2292C= XP_006711979.1:p.Leu764=
XM_011532473.1:c.2292C= XP_011530775.1:p.Leu764=
XM_011532474.1:c.2292C= XP_011530776.1:p.Leu764=
XM_006711916.3:c.2292C= XP_006711979.1:p.Leu764=
XM_017003117.1:c.2214C= XP_016858606.1:p.Leu738=
XR_002958896.1:n.2334C=
NM_133259.4:c.2292C= MANE Select NP_573566.2:p.Leu764=