Canonical Allele Identifier: CA2493977944
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43899286G= , CM000664.2:g.43899286G= GRCh38
NC_000002.11:g.44126425G= , CM000664.1:g.44126425G= GRCh37
NC_000002.10:g.43979929G= NCBI36
NG_008247.1:g.101720C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000419884.6:c.189C=
ENST00000472420.6:n.837C=
ENST00000483489.2:n.189C=
ENST00000681993.1:n.1310C=
ENST00000682303.1:c.*3544C= ENSP00000508325.1:n.*3544C=
ENST00000682308.1:c.3758C= ENSP00000507056.1:p.Pro1253=
ENST00000682434.1:n.1309C=
ENST00000682480.1:c.3776C= ENSP00000508344.1:p.Pro1259=
ENST00000682546.1:c.3755C= ENSP00000508188.1:p.Pro1252=
ENST00000682585.1:c.3758C= ENSP00000506885.1:p.Pro1253=
ENST00000682595.1:n.4342C=
ENST00000682607.1:c.2176C=
ENST00000682612.1:c.610C=
ENST00000682779.1:c.3749C= ENSP00000507947.1:p.Pro1250=
ENST00000682845.1:n.2860C=
ENST00000682885.1:c.3713C= ENSP00000508036.1:p.Pro1238=
ENST00000682933.1:n.3832C=
ENST00000683002.1:c.610C=
ENST00000683072.1:n.4342C=
ENST00000683080.1:n.1377C=
ENST00000683125.1:c.3866C= ENSP00000507939.1:p.Pro1289=
ENST00000683213.1:c.3761C= ENSP00000507751.1:p.Pro1254=
ENST00000683220.1:c.3788C= ENSP00000507151.1:p.Pro1263=
ENST00000683329.1:n.4561C=
ENST00000683346.1:c.*3633C= ENSP00000507458.1:n.*3633C=
ENST00000683409.1:n.2365C=
ENST00000683459.1:n.4345C=
ENST00000683528.1:c.686C=
ENST00000683590.1:c.3506C= ENSP00000506820.1:p.Pro1169=
ENST00000683623.1:c.3665C= ENSP00000507702.1:p.Pro1222=
ENST00000683645.1:n.4309C=
ENST00000683796.1:c.*3630C= ENSP00000508221.1:n.*3630C=
ENST00000683802.1:n.6683C=
ENST00000683833.1:c.3749C= ENSP00000506852.1:p.Pro1250=
ENST00000683994.1:c.3758C= ENSP00000507181.1:p.Pro1253=
ENST00000684290.1:c.*1294C= ENSP00000507243.1:n.*1294C=
ENST00000684306.1:c.*3671C= ENSP00000508384.1:n.*3671C=
ENST00000684341.1:n.3778C=
ENST00000684383.1:c.*3396C= ENSP00000506863.1:n.*3396C=
ENST00000684418.1:n.4939C=
ENST00000684433.1:n.142C=
ENST00000684454.1:n.3108C=
ENST00000684619.1:c.*3630C= ENSP00000508088.1:n.*3630C=
ENST00000684743.1:n.6503C=
ENST00000260665.12:c.3758C= MANE Select ENSP00000260665.7:p.Pro1253=
ENST00000260665.11:c.3758C= ENSP00000260665.7:p.Pro1253=
ENST00000463456.5:n.2801C=
ENST00000472420.5:n.155C=
ENST00000483489.1:n.232C=
NM_133259.3:c.3758C= NP_573566.2:p.Pro1253=
XM_006711915.2:c.3680C= XP_006711978.1:p.Pro1227=
XM_011532473.1:c.3758C= XP_011530775.1:p.Pro1253=
XM_011532474.1:c.3758C= XP_011530776.1:p.Pro1253=
XM_017003117.1:c.3680C= XP_016858606.1:p.Pro1227=
XR_002958896.1:n.3800C=
NM_133259.4:c.3758C= MANE Select NP_573566.2:p.Pro1253=