Canonical Allele Identifier: CA2493977933
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43899264T= , CM000664.2:g.43899264T= GRCh38
NC_000002.11:g.44126403T= , CM000664.1:g.44126403T= GRCh37
NC_000002.10:g.43979907T= NCBI36
NG_008247.1:g.101742A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000419884.6:c.211A=
ENST00000472420.6:n.859A=
ENST00000483489.2:n.211A=
ENST00000681993.1:n.1332A=
ENST00000682303.1:c.*3566A= ENSP00000508325.1:n.*3566A=
ENST00000682308.1:c.3780A= ENSP00000507056.1:p.Gln1260=
ENST00000682434.1:n.1331A=
ENST00000682480.1:c.3798A= ENSP00000508344.1:p.Gln1266=
ENST00000682546.1:c.3777A= ENSP00000508188.1:p.Gln1259=
ENST00000682585.1:c.3780A= ENSP00000506885.1:p.Gln1260=
ENST00000682595.1:n.4364A=
ENST00000682607.1:c.2198A=
ENST00000682612.1:c.632A=
ENST00000682779.1:c.3771A= ENSP00000507947.1:p.Gln1257=
ENST00000682845.1:n.2882A=
ENST00000682885.1:c.3735A= ENSP00000508036.1:p.Gln1245=
ENST00000682933.1:n.3854A=
ENST00000683002.1:c.632A=
ENST00000683072.1:n.4364A=
ENST00000683080.1:n.1399A=
ENST00000683125.1:c.3888A= ENSP00000507939.1:p.Gln1296=
ENST00000683213.1:c.3783A= ENSP00000507751.1:p.Gln1261=
ENST00000683220.1:c.3810A= ENSP00000507151.1:p.Gln1270=
ENST00000683329.1:n.4583A=
ENST00000683346.1:c.*3655A= ENSP00000507458.1:n.*3655A=
ENST00000683409.1:n.2387A=
ENST00000683459.1:n.4367A=
ENST00000683528.1:c.708A=
ENST00000683590.1:c.3528A= ENSP00000506820.1:p.Gln1176=
ENST00000683623.1:c.3687A= ENSP00000507702.1:p.Gln1229=
ENST00000683645.1:n.4331A=
ENST00000683796.1:c.*3652A= ENSP00000508221.1:n.*3652A=
ENST00000683802.1:n.6705A=
ENST00000683833.1:c.3771A= ENSP00000506852.1:p.Gln1257=
ENST00000683994.1:c.3780A= ENSP00000507181.1:p.Gln1260=
ENST00000684290.1:c.*1316A= ENSP00000507243.1:n.*1316A=
ENST00000684306.1:c.*3693A= ENSP00000508384.1:n.*3693A=
ENST00000684341.1:n.3800A=
ENST00000684383.1:c.*3418A= ENSP00000506863.1:n.*3418A=
ENST00000684418.1:n.4961A=
ENST00000684433.1:n.164A=
ENST00000684454.1:n.3130A=
ENST00000684619.1:c.*3652A= ENSP00000508088.1:n.*3652A=
ENST00000684743.1:n.6525A=
ENST00000260665.12:c.3780A= MANE Select ENSP00000260665.7:p.Gln1260=
ENST00000260665.11:c.3780A= ENSP00000260665.7:p.Gln1260=
ENST00000419884.5:c.21A= ENSP00000414207.1:p.Gln7=
ENST00000463456.5:n.2823A=
ENST00000472420.5:n.177A=
ENST00000483489.1:n.254A=
NM_133259.3:c.3780A= NP_573566.2:p.Gln1260=
XM_006711915.2:c.3702A= XP_006711978.1:p.Gln1234=
XM_011532473.1:c.3780A= XP_011530775.1:p.Gln1260=
XM_011532474.1:c.3780A= XP_011530776.1:p.Gln1260=
XM_017003117.1:c.3702A= XP_016858606.1:p.Gln1234=
XR_002958896.1:n.3822A=
NM_133259.4:c.3780A= MANE Select NP_573566.2:p.Gln1260=