Canonical Allele Identifier: CA2493988090
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43918043G= , CM000664.2:g.43918043G= GRCh38
NC_000002.11:g.44145182G= , CM000664.1:g.44145182G= GRCh37
NC_000002.10:g.43998686G= NCBI36
NG_008247.1:g.82963C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681993.1:n.682C=
ENST00000682295.1:c.303+213C= ENSP00000507499.1:n.303+213C=
ENST00000682303.1:c.*2916C= ENSP00000508325.1:n.*2916C=
ENST00000682308.1:c.3130C= ENSP00000507056.1:p.Arg1044=
ENST00000682480.1:c.3148C= ENSP00000508344.1:p.Arg1050=
ENST00000682546.1:c.3127C= ENSP00000508188.1:p.Arg1043=
ENST00000682585.1:c.3130C= ENSP00000506885.1:p.Arg1044=
ENST00000682595.1:n.3714C=
ENST00000682607.1:c.1548C=
ENST00000682779.1:c.3121C= ENSP00000507947.1:p.Arg1041=
ENST00000682845.1:n.2232C=
ENST00000682885.1:c.3085C= ENSP00000508036.1:p.Arg1029=
ENST00000682933.1:n.3204C=
ENST00000683072.1:n.3714C=
ENST00000683080.1:n.749C=
ENST00000683125.1:c.3238C= ENSP00000507939.1:p.Arg1080=
ENST00000683213.1:c.3133C= ENSP00000507751.1:p.Arg1045=
ENST00000683220.1:c.3160C= ENSP00000507151.1:p.Arg1054=
ENST00000683329.1:n.3933C=
ENST00000683346.1:c.*3005C= ENSP00000507458.1:n.*3005C=
ENST00000683409.1:n.1737C=
ENST00000683459.1:n.3717C=
ENST00000683590.1:c.2897-5485C= ENSP00000506820.1:n.2897-5485C=
ENST00000683623.1:c.3037C= ENSP00000507702.1:p.Arg1013=
ENST00000683645.1:n.3681C=
ENST00000683796.1:c.*3002C= ENSP00000508221.1:n.*3002C=
ENST00000683802.1:n.6055C=
ENST00000683833.1:c.3121C= ENSP00000506852.1:p.Arg1041=
ENST00000683994.1:c.3130C= ENSP00000507181.1:p.Arg1044=
ENST00000684290.1:c.*666C= ENSP00000507243.1:n.*666C=
ENST00000684306.1:c.*3043C= ENSP00000508384.1:n.*3043C=
ENST00000684341.1:n.3150C=
ENST00000684383.1:c.*2768C= ENSP00000506863.1:n.*2768C=
ENST00000684619.1:c.*3002C= ENSP00000508088.1:n.*3002C=
ENST00000684705.1:n.251C=
ENST00000684743.1:n.4161C=
ENST00000260665.12:c.3130C= MANE Select ENSP00000260665.7:p.Arg1044=
ENST00000260665.11:c.3130C= ENSP00000260665.7:p.Arg1044=
NM_133259.3:c.3130C= NP_573566.2:p.Arg1044=
XM_006711915.2:c.3052C= XP_006711978.1:p.Arg1018=
XM_006711916.2:c.3130C= XP_006711979.1:p.Arg1044=
XM_011532473.1:c.3130C= XP_011530775.1:p.Arg1044=
XM_011532474.1:c.3130C= XP_011530776.1:p.Arg1044=
XM_006711916.3:c.3130C= XP_006711979.1:p.Arg1044=
XM_017003117.1:c.3052C= XP_016858606.1:p.Arg1018=
XR_002958896.1:n.3172C=
NM_133259.4:c.3130C= MANE Select NP_573566.2:p.Arg1044=