Canonical Allele Identifier: CA2493975255
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43894561G= , CM000664.2:g.43894561G= GRCh38
NC_000002.11:g.44121700G= , CM000664.1:g.44121700G= GRCh37
NC_000002.10:g.43975204G= NCBI36
NG_008247.1:g.106445C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000419884.6:c.599C=
ENST00000681993.1:n.1521C=
ENST00000682154.1:n.1403C=
ENST00000682303.1:c.*3680C= ENSP00000508325.1:n.*3680C=
ENST00000682308.1:c.3894C= ENSP00000507056.1:p.Ser1298=
ENST00000682434.1:n.3524C=
ENST00000682480.1:c.3987C= ENSP00000508344.1:p.Ser1329=
ENST00000682546.1:c.3966C= ENSP00000508188.1:p.Ser1322=
ENST00000682585.1:c.*97C= ENSP00000506885.1:n.*97C=
ENST00000682607.1:c.2712C=
ENST00000682612.1:c.752+2073C=
ENST00000682696.1:c.69C= ENSP00000508411.1:p.Ser23=
ENST00000682779.1:c.3960C= ENSP00000507947.1:p.Ser1320=
ENST00000682885.1:c.3924C= ENSP00000508036.1:p.Ser1308=
ENST00000682933.1:n.4169C=
ENST00000683002.1:c.821C=
ENST00000683072.1:n.4553C=
ENST00000683080.1:n.1588C=
ENST00000683096.1:n.2410C=
ENST00000683125.1:c.4077C= ENSP00000507939.1:p.Ser1359=
ENST00000683213.1:c.3972C= ENSP00000507751.1:p.Ser1324=
ENST00000683220.1:c.3999C= ENSP00000507151.1:p.Ser1333=
ENST00000683329.1:n.4772C=
ENST00000683346.1:c.*3844C= ENSP00000507458.1:n.*3844C=
ENST00000683409.1:n.2501C=
ENST00000683459.1:n.4556C=
ENST00000683590.1:c.3642C= ENSP00000506820.1:p.Ser1214=
ENST00000683623.1:c.3876C= ENSP00000507702.1:p.Ser1292=
ENST00000683796.1:c.*3766C= ENSP00000508221.1:n.*3766C=
ENST00000683833.1:c.3885C= ENSP00000506852.1:p.Ser1295=
ENST00000683994.1:c.*82C= ENSP00000507181.1:n.*82C=
ENST00000684290.1:c.*1430C= ENSP00000507243.1:n.*1430C=
ENST00000684306.1:c.*3882C= ENSP00000508384.1:n.*3882C=
ENST00000684383.1:c.*3607C= ENSP00000506863.1:n.*3607C=
ENST00000684418.1:n.5150C=
ENST00000684433.1:n.353C=
ENST00000684454.1:n.7833C=
ENST00000684619.1:c.*3841C= ENSP00000508088.1:n.*3841C=
ENST00000684743.1:n.6714C=
ENST00000260665.12:c.3969C= MANE Select ENSP00000260665.7:p.Ser1323=
ENST00000260665.11:c.3969C= ENSP00000260665.7:p.Ser1323=
ENST00000419884.5:c.210C= ENSP00000414207.1:p.Ser70=
ENST00000463456.5:n.3012C=
NM_133259.3:c.3969C= NP_573566.2:p.Ser1323=
XM_006711915.2:c.3891C= XP_006711978.1:p.Ser1297=
XM_011532473.1:c.3894C= XP_011530775.1:p.Ser1298=
XM_011532474.1:c.3969C= XP_011530776.1:p.Ser1323=
XM_017003117.1:c.3816C= XP_016858606.1:p.Ser1272=
XR_002958896.1:n.4011C=
NM_133259.4:c.3969C= MANE Select NP_573566.2:p.Ser1323=