Canonical Allele Identifier: CA2493975257
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43894565T= , CM000664.2:g.43894565T= GRCh38
NC_000002.11:g.44121704T= , CM000664.1:g.44121704T= GRCh37
NC_000002.10:g.43975208T= NCBI36
NG_008247.1:g.106441A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000419884.6:c.595A=
ENST00000681993.1:n.1517A=
ENST00000682154.1:n.1399A=
ENST00000682303.1:c.*3676A= ENSP00000508325.1:n.*3676A=
ENST00000682308.1:c.3890A= ENSP00000507056.1:p.Asn1297=
ENST00000682434.1:n.3520A=
ENST00000682480.1:c.3983A= ENSP00000508344.1:p.Asn1328=
ENST00000682546.1:c.3962A= ENSP00000508188.1:p.Asn1321=
ENST00000682585.1:c.*93A= ENSP00000506885.1:n.*93A=
ENST00000682607.1:c.2708A=
ENST00000682612.1:c.752+2069A=
ENST00000682696.1:c.65A= ENSP00000508411.1:p.Asn22=
ENST00000682779.1:c.3956A= ENSP00000507947.1:p.Asn1319=
ENST00000682885.1:c.3920A= ENSP00000508036.1:p.Asn1307=
ENST00000682933.1:n.4165A=
ENST00000683002.1:c.817A=
ENST00000683072.1:n.4549A=
ENST00000683080.1:n.1584A=
ENST00000683096.1:n.2406A=
ENST00000683125.1:c.4073A= ENSP00000507939.1:p.Asn1358=
ENST00000683213.1:c.3968A= ENSP00000507751.1:p.Asn1323=
ENST00000683220.1:c.3995A= ENSP00000507151.1:p.Asn1332=
ENST00000683329.1:n.4768A=
ENST00000683346.1:c.*3840A= ENSP00000507458.1:n.*3840A=
ENST00000683409.1:n.2497A=
ENST00000683459.1:n.4552A=
ENST00000683590.1:c.3638A= ENSP00000506820.1:p.Asn1213=
ENST00000683623.1:c.3872A= ENSP00000507702.1:p.Asn1291=
ENST00000683796.1:c.*3762A= ENSP00000508221.1:n.*3762A=
ENST00000683833.1:c.3881A= ENSP00000506852.1:p.Asn1294=
ENST00000683994.1:c.*78A= ENSP00000507181.1:n.*78A=
ENST00000684290.1:c.*1426A= ENSP00000507243.1:n.*1426A=
ENST00000684306.1:c.*3878A= ENSP00000508384.1:n.*3878A=
ENST00000684383.1:c.*3603A= ENSP00000506863.1:n.*3603A=
ENST00000684418.1:n.5146A=
ENST00000684433.1:n.349A=
ENST00000684454.1:n.7829A=
ENST00000684619.1:c.*3837A= ENSP00000508088.1:n.*3837A=
ENST00000684743.1:n.6710A=
ENST00000260665.12:c.3965A= MANE Select ENSP00000260665.7:p.Asn1322=
ENST00000260665.11:c.3965A= ENSP00000260665.7:p.Asn1322=
ENST00000419884.5:c.206A= ENSP00000414207.1:p.Asn69=
ENST00000463456.5:n.3008A=
NM_133259.3:c.3965A= NP_573566.2:p.Asn1322=
XM_006711915.2:c.3887A= XP_006711978.1:p.Asn1296=
XM_011532473.1:c.3890A= XP_011530775.1:p.Asn1297=
XM_011532474.1:c.3965A= XP_011530776.1:p.Asn1322=
XM_017003117.1:c.3812A= XP_016858606.1:p.Asn1271=
XR_002958896.1:n.4007A=
NM_133259.4:c.3965A= MANE Select NP_573566.2:p.Asn1322=