Canonical Allele Identifier: CA2493977947
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43899297T= , CM000664.2:g.43899297T= GRCh38
NC_000002.11:g.44126436T= , CM000664.1:g.44126436T= GRCh37
NC_000002.10:g.43979940T= NCBI36
NG_008247.1:g.101709A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000419884.6:c.178A=
ENST00000472420.6:n.826A=
ENST00000483489.2:n.178A=
ENST00000681993.1:n.1299A=
ENST00000682303.1:c.*3533A= ENSP00000508325.1:n.*3533A=
ENST00000682308.1:c.3747A= ENSP00000507056.1:p.Ala1249=
ENST00000682434.1:n.1298A=
ENST00000682480.1:c.3765A= ENSP00000508344.1:p.Ala1255=
ENST00000682546.1:c.3744A= ENSP00000508188.1:p.Ala1248=
ENST00000682585.1:c.3747A= ENSP00000506885.1:p.Ala1249=
ENST00000682595.1:n.4331A=
ENST00000682607.1:c.2165A=
ENST00000682612.1:c.599A=
ENST00000682779.1:c.3738A= ENSP00000507947.1:p.Ala1246=
ENST00000682845.1:n.2849A=
ENST00000682885.1:c.3702A= ENSP00000508036.1:p.Ala1234=
ENST00000682933.1:n.3821A=
ENST00000683002.1:c.599A=
ENST00000683072.1:n.4331A=
ENST00000683080.1:n.1366A=
ENST00000683125.1:c.3855A= ENSP00000507939.1:p.Ala1285=
ENST00000683213.1:c.3750A= ENSP00000507751.1:p.Ala1250=
ENST00000683220.1:c.3777A= ENSP00000507151.1:p.Ala1259=
ENST00000683329.1:n.4550A=
ENST00000683346.1:c.*3622A= ENSP00000507458.1:n.*3622A=
ENST00000683409.1:n.2354A=
ENST00000683459.1:n.4334A=
ENST00000683528.1:c.675A=
ENST00000683590.1:c.3495A= ENSP00000506820.1:p.Ala1165=
ENST00000683623.1:c.3654A= ENSP00000507702.1:p.Ala1218=
ENST00000683645.1:n.4298A=
ENST00000683796.1:c.*3619A= ENSP00000508221.1:n.*3619A=
ENST00000683802.1:n.6672A=
ENST00000683833.1:c.3738A= ENSP00000506852.1:p.Ala1246=
ENST00000683994.1:c.3747A= ENSP00000507181.1:p.Ala1249=
ENST00000684290.1:c.*1283A= ENSP00000507243.1:n.*1283A=
ENST00000684306.1:c.*3660A= ENSP00000508384.1:n.*3660A=
ENST00000684341.1:n.3767A=
ENST00000684383.1:c.*3385A= ENSP00000506863.1:n.*3385A=
ENST00000684418.1:n.4928A=
ENST00000684433.1:n.131A=
ENST00000684454.1:n.3097A=
ENST00000684619.1:c.*3619A= ENSP00000508088.1:n.*3619A=
ENST00000684743.1:n.6492A=
ENST00000260665.12:c.3747A= MANE Select ENSP00000260665.7:p.Ala1249=
ENST00000260665.11:c.3747A= ENSP00000260665.7:p.Ala1249=
ENST00000463456.5:n.2790A=
ENST00000472420.5:n.144A=
ENST00000483489.1:n.221A=
NM_133259.3:c.3747A= NP_573566.2:p.Ala1249=
XM_006711915.2:c.3669A= XP_006711978.1:p.Ala1223=
XM_011532473.1:c.3747A= XP_011530775.1:p.Ala1249=
XM_011532474.1:c.3747A= XP_011530776.1:p.Ala1249=
XM_017003117.1:c.3669A= XP_016858606.1:p.Ala1223=
XR_002958896.1:n.3789A=
NM_133259.4:c.3747A= MANE Select NP_573566.2:p.Ala1249=