Canonical Allele Identifier: CA2493977950
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43899303C= , CM000664.2:g.43899303C= GRCh38
NC_000002.11:g.44126442C= , CM000664.1:g.44126442C= GRCh37
NC_000002.10:g.43979946C= NCBI36
NG_008247.1:g.101703G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000419884.6:c.172G=
ENST00000472420.6:n.820G=
ENST00000483489.2:n.172G=
ENST00000681993.1:n.1293G=
ENST00000682303.1:c.*3527G= ENSP00000508325.1:n.*3527G=
ENST00000682308.1:c.3741G= ENSP00000507056.1:p.Gln1247=
ENST00000682434.1:n.1292G=
ENST00000682480.1:c.3759G= ENSP00000508344.1:p.Gln1253=
ENST00000682546.1:c.3738G= ENSP00000508188.1:p.Gln1246=
ENST00000682585.1:c.3741G= ENSP00000506885.1:p.Gln1247=
ENST00000682595.1:n.4325G=
ENST00000682607.1:c.2159G=
ENST00000682612.1:c.593G=
ENST00000682779.1:c.3732G= ENSP00000507947.1:p.Gln1244=
ENST00000682845.1:n.2843G=
ENST00000682885.1:c.3696G= ENSP00000508036.1:p.Gln1232=
ENST00000682933.1:n.3815G=
ENST00000683002.1:c.593G=
ENST00000683072.1:n.4325G=
ENST00000683080.1:n.1360G=
ENST00000683125.1:c.3849G= ENSP00000507939.1:p.Gln1283=
ENST00000683213.1:c.3744G= ENSP00000507751.1:p.Gln1248=
ENST00000683220.1:c.3771G= ENSP00000507151.1:p.Gln1257=
ENST00000683329.1:n.4544G=
ENST00000683346.1:c.*3616G= ENSP00000507458.1:n.*3616G=
ENST00000683409.1:n.2348G=
ENST00000683459.1:n.4328G=
ENST00000683528.1:c.669G=
ENST00000683590.1:c.3489G= ENSP00000506820.1:p.Gln1163=
ENST00000683623.1:c.3648G= ENSP00000507702.1:p.Gln1216=
ENST00000683645.1:n.4292G=
ENST00000683796.1:c.*3613G= ENSP00000508221.1:n.*3613G=
ENST00000683802.1:n.6666G=
ENST00000683833.1:c.3732G= ENSP00000506852.1:p.Gln1244=
ENST00000683994.1:c.3741G= ENSP00000507181.1:p.Gln1247=
ENST00000684290.1:c.*1277G= ENSP00000507243.1:n.*1277G=
ENST00000684306.1:c.*3654G= ENSP00000508384.1:n.*3654G=
ENST00000684341.1:n.3761G=
ENST00000684383.1:c.*3379G= ENSP00000506863.1:n.*3379G=
ENST00000684418.1:n.4922G=
ENST00000684433.1:n.125G=
ENST00000684454.1:n.3091G=
ENST00000684619.1:c.*3613G= ENSP00000508088.1:n.*3613G=
ENST00000684743.1:n.6486G=
ENST00000260665.12:c.3741G= MANE Select ENSP00000260665.7:p.Gln1247=
ENST00000260665.11:c.3741G= ENSP00000260665.7:p.Gln1247=
ENST00000463456.5:n.2784G=
ENST00000472420.5:n.138G=
ENST00000483489.1:n.215G=
NM_133259.3:c.3741G= NP_573566.2:p.Gln1247=
XM_006711915.2:c.3663G= XP_006711978.1:p.Gln1221=
XM_011532473.1:c.3741G= XP_011530775.1:p.Gln1247=
XM_011532474.1:c.3741G= XP_011530776.1:p.Gln1247=
XM_017003117.1:c.3663G= XP_016858606.1:p.Gln1221=
XR_002958896.1:n.3783G=
NM_133259.4:c.3741G= MANE Select NP_573566.2:p.Gln1247=