Canonical Allele Identifier: CA2493977921
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43899233T= , CM000664.2:g.43899233T= GRCh38
NC_000002.11:g.44126372T= , CM000664.1:g.44126372T= GRCh37
NC_000002.10:g.43979876T= NCBI36
NG_008247.1:g.101773A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000419884.6:c.242A=
ENST00000472420.6:n.890A=
ENST00000483489.2:n.242A=
ENST00000681993.1:n.1363A=
ENST00000682303.1:c.*3597A= ENSP00000508325.1:n.*3597A=
ENST00000682308.1:c.3811A= ENSP00000507056.1:p.Arg1271=
ENST00000682434.1:n.1362A=
ENST00000682480.1:c.3829A= ENSP00000508344.1:p.Arg1277=
ENST00000682546.1:c.3808A= ENSP00000508188.1:p.Arg1270=
ENST00000682585.1:c.3811A= ENSP00000506885.1:p.Arg1271=
ENST00000682595.1:n.4395A=
ENST00000682607.1:c.2229A=
ENST00000682612.1:c.663A=
ENST00000682779.1:c.3802A= ENSP00000507947.1:p.Arg1268=
ENST00000682885.1:c.3766A= ENSP00000508036.1:p.Arg1256=
ENST00000682933.1:n.3885A=
ENST00000683002.1:c.663A=
ENST00000683072.1:n.4395A=
ENST00000683080.1:n.1430A=
ENST00000683125.1:c.3919A= ENSP00000507939.1:p.Arg1307=
ENST00000683213.1:c.3814A= ENSP00000507751.1:p.Arg1272=
ENST00000683220.1:c.3841A= ENSP00000507151.1:p.Arg1281=
ENST00000683329.1:n.4614A=
ENST00000683346.1:c.*3686A= ENSP00000507458.1:n.*3686A=
ENST00000683409.1:n.2418A=
ENST00000683459.1:n.4398A=
ENST00000683528.1:c.739A=
ENST00000683590.1:c.3559A= ENSP00000506820.1:p.Arg1187=
ENST00000683623.1:c.3718A= ENSP00000507702.1:p.Arg1240=
ENST00000683645.1:n.4362A=
ENST00000683796.1:c.*3683A= ENSP00000508221.1:n.*3683A=
ENST00000683802.1:n.6736A=
ENST00000683833.1:c.3802A= ENSP00000506852.1:p.Arg1268=
ENST00000683994.1:c.3811A= ENSP00000507181.1:p.Arg1271=
ENST00000684290.1:c.*1347A= ENSP00000507243.1:n.*1347A=
ENST00000684306.1:c.*3724A= ENSP00000508384.1:n.*3724A=
ENST00000684341.1:n.3831A=
ENST00000684383.1:c.*3449A= ENSP00000506863.1:n.*3449A=
ENST00000684418.1:n.4992A=
ENST00000684433.1:n.195A=
ENST00000684454.1:n.3161A=
ENST00000684619.1:c.*3683A= ENSP00000508088.1:n.*3683A=
ENST00000684743.1:n.6556A=
ENST00000260665.12:c.3811A= MANE Select ENSP00000260665.7:p.Arg1271=
ENST00000260665.11:c.3811A= ENSP00000260665.7:p.Arg1271=
ENST00000419884.5:c.52A= ENSP00000414207.1:p.Arg18=
ENST00000463456.5:n.2854A=
ENST00000472420.5:n.208A=
ENST00000483489.1:n.285A=
NM_133259.3:c.3811A= NP_573566.2:p.Arg1271=
XM_006711915.2:c.3733A= XP_006711978.1:p.Arg1245=
XM_011532473.1:c.3811A= XP_011530775.1:p.Arg1271=
XM_011532474.1:c.3811A= XP_011530776.1:p.Arg1271=
XM_017003117.1:c.3733A= XP_016858606.1:p.Arg1245=
XR_002958896.1:n.3853A=
NM_133259.4:c.3811A= MANE Select NP_573566.2:p.Arg1271=