Canonical Allele Identifier: CA2493977954
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43899315T= , CM000664.2:g.43899315T= GRCh38
NC_000002.11:g.44126454T= , CM000664.1:g.44126454T= GRCh37
NC_000002.10:g.43979958T= NCBI36
NG_008247.1:g.101691A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000419884.6:c.160A=
ENST00000472420.6:n.808A=
ENST00000483489.2:n.160A=
ENST00000681993.1:n.1281A=
ENST00000682303.1:c.*3515A= ENSP00000508325.1:n.*3515A=
ENST00000682308.1:c.3729A= ENSP00000507056.1:p.Arg1243=
ENST00000682434.1:n.1280A=
ENST00000682480.1:c.3747A= ENSP00000508344.1:p.Arg1249=
ENST00000682546.1:c.3726A= ENSP00000508188.1:p.Arg1242=
ENST00000682585.1:c.3729A= ENSP00000506885.1:p.Arg1243=
ENST00000682595.1:n.4313A=
ENST00000682607.1:c.2147A=
ENST00000682612.1:c.581A=
ENST00000682779.1:c.3720A= ENSP00000507947.1:p.Arg1240=
ENST00000682845.1:n.2831A=
ENST00000682885.1:c.3684A= ENSP00000508036.1:p.Arg1228=
ENST00000682933.1:n.3803A=
ENST00000683002.1:c.581A=
ENST00000683072.1:n.4313A=
ENST00000683080.1:n.1348A=
ENST00000683125.1:c.3837A= ENSP00000507939.1:p.Arg1279=
ENST00000683213.1:c.3732A= ENSP00000507751.1:p.Arg1244=
ENST00000683220.1:c.3759A= ENSP00000507151.1:p.Arg1253=
ENST00000683329.1:n.4532A=
ENST00000683346.1:c.*3604A= ENSP00000507458.1:n.*3604A=
ENST00000683409.1:n.2336A=
ENST00000683459.1:n.4316A=
ENST00000683528.1:c.657A=
ENST00000683590.1:c.3477A= ENSP00000506820.1:p.Arg1159=
ENST00000683623.1:c.3636A= ENSP00000507702.1:p.Arg1212=
ENST00000683645.1:n.4280A=
ENST00000683796.1:c.*3601A= ENSP00000508221.1:n.*3601A=
ENST00000683802.1:n.6654A=
ENST00000683833.1:c.3720A= ENSP00000506852.1:p.Arg1240=
ENST00000683994.1:c.3729A= ENSP00000507181.1:p.Arg1243=
ENST00000684290.1:c.*1265A= ENSP00000507243.1:n.*1265A=
ENST00000684306.1:c.*3642A= ENSP00000508384.1:n.*3642A=
ENST00000684341.1:n.3749A=
ENST00000684383.1:c.*3367A= ENSP00000506863.1:n.*3367A=
ENST00000684418.1:n.4910A=
ENST00000684433.1:n.113A=
ENST00000684454.1:n.3079A=
ENST00000684619.1:c.*3601A= ENSP00000508088.1:n.*3601A=
ENST00000684743.1:n.6474A=
ENST00000260665.12:c.3729A= MANE Select ENSP00000260665.7:p.Arg1243=
ENST00000260665.11:c.3729A= ENSP00000260665.7:p.Arg1243=
ENST00000463456.5:n.2772A=
ENST00000472420.5:n.126A=
ENST00000483489.1:n.203A=
NM_133259.3:c.3729A= NP_573566.2:p.Arg1243=
XM_006711915.2:c.3651A= XP_006711978.1:p.Arg1217=
XM_011532473.1:c.3729A= XP_011530775.1:p.Arg1243=
XM_011532474.1:c.3729A= XP_011530776.1:p.Arg1243=
XM_017003117.1:c.3651A= XP_016858606.1:p.Arg1217=
XR_002958896.1:n.3771A=
NM_133259.4:c.3729A= MANE Select NP_573566.2:p.Arg1243=