Canonical Allele Identifier: CA2493975276
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43894614A= , CM000664.2:g.43894614A= GRCh38
NC_000002.11:g.44121753A= , CM000664.1:g.44121753A= GRCh37
NC_000002.10:g.43975257A= NCBI36
NG_008247.1:g.106392T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000419884.6:c.546T=
ENST00000681993.1:n.1468T=
ENST00000682154.1:n.1350T=
ENST00000682303.1:c.*3627T= ENSP00000508325.1:n.*3627T=
ENST00000682308.1:c.3841T= ENSP00000507056.1:p.Ser1281=
ENST00000682434.1:n.3471T=
ENST00000682480.1:c.3934T= ENSP00000508344.1:p.Ser1312=
ENST00000682546.1:c.3913T= ENSP00000508188.1:p.Ser1305=
ENST00000682585.1:c.*44T= ENSP00000506885.1:n.*44T=
ENST00000682607.1:c.2659T=
ENST00000682612.1:c.752+2020T=
ENST00000682696.1:c.16T= ENSP00000508411.1:p.Ser6=
ENST00000682779.1:c.3907T= ENSP00000507947.1:p.Ser1303=
ENST00000682885.1:c.3871T= ENSP00000508036.1:p.Ser1291=
ENST00000682933.1:n.4116T=
ENST00000683002.1:c.768T=
ENST00000683072.1:n.4500T=
ENST00000683080.1:n.1535T=
ENST00000683096.1:n.2357T=
ENST00000683125.1:c.4024T= ENSP00000507939.1:p.Ser1342=
ENST00000683213.1:c.3919T= ENSP00000507751.1:p.Ser1307=
ENST00000683220.1:c.3946T= ENSP00000507151.1:p.Ser1316=
ENST00000683329.1:n.4719T=
ENST00000683346.1:c.*3791T= ENSP00000507458.1:n.*3791T=
ENST00000683409.1:n.2448T=
ENST00000683459.1:n.4503T=
ENST00000683590.1:c.3589T= ENSP00000506820.1:p.Ser1197=
ENST00000683623.1:c.3823T= ENSP00000507702.1:p.Ser1275=
ENST00000683796.1:c.*3713T= ENSP00000508221.1:n.*3713T=
ENST00000683833.1:c.3832T= ENSP00000506852.1:p.Ser1278=
ENST00000683994.1:c.*29T= ENSP00000507181.1:n.*29T=
ENST00000684290.1:c.*1377T= ENSP00000507243.1:n.*1377T=
ENST00000684306.1:c.*3829T= ENSP00000508384.1:n.*3829T=
ENST00000684383.1:c.*3554T= ENSP00000506863.1:n.*3554T=
ENST00000684418.1:n.5097T=
ENST00000684433.1:n.300T=
ENST00000684454.1:n.7780T=
ENST00000684619.1:c.*3788T= ENSP00000508088.1:n.*3788T=
ENST00000684743.1:n.6661T=
ENST00000260665.12:c.3916T= MANE Select ENSP00000260665.7:p.Ser1306=
ENST00000260665.11:c.3916T= ENSP00000260665.7:p.Ser1306=
ENST00000419884.5:c.157T= ENSP00000414207.1:p.Ser53=
ENST00000463456.5:n.2959T=
NM_133259.3:c.3916T= NP_573566.2:p.Ser1306=
XM_006711915.2:c.3838T= XP_006711978.1:p.Ser1280=
XM_011532473.1:c.3841T= XP_011530775.1:p.Ser1281=
XM_011532474.1:c.3916T= XP_011530776.1:p.Ser1306=
XM_017003117.1:c.3763T= XP_016858606.1:p.Ser1255=
XR_002958896.1:n.3958T=
NM_133259.4:c.3916T= MANE Select NP_573566.2:p.Ser1306=