Canonical Allele Identifier: CA2493988104
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43918078T= , CM000664.2:g.43918078T= GRCh38
NC_000002.11:g.44145217T= , CM000664.1:g.44145217T= GRCh37
NC_000002.10:g.43998721T= NCBI36
NG_008247.1:g.82928A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681993.1:n.647A=
ENST00000682295.1:c.303+178A= ENSP00000507499.1:n.303+178A=
ENST00000682303.1:c.*2881A= ENSP00000508325.1:n.*2881A=
ENST00000682308.1:c.3095A= ENSP00000507056.1:p.Glu1032=
ENST00000682480.1:c.3113A= ENSP00000508344.1:p.Glu1038=
ENST00000682546.1:c.3092A= ENSP00000508188.1:p.Glu1031=
ENST00000682585.1:c.3095A= ENSP00000506885.1:p.Glu1032=
ENST00000682595.1:n.3679A=
ENST00000682607.1:c.1513A=
ENST00000682779.1:c.3086A= ENSP00000507947.1:p.Glu1029=
ENST00000682845.1:n.2197A=
ENST00000682885.1:c.3050A= ENSP00000508036.1:p.Glu1017=
ENST00000682933.1:n.3169A=
ENST00000683072.1:n.3679A=
ENST00000683080.1:n.714A=
ENST00000683125.1:c.3203A= ENSP00000507939.1:p.Glu1068=
ENST00000683213.1:c.3098A= ENSP00000507751.1:p.Glu1033=
ENST00000683220.1:c.3125A= ENSP00000507151.1:p.Glu1042=
ENST00000683329.1:n.3898A=
ENST00000683346.1:c.*2970A= ENSP00000507458.1:n.*2970A=
ENST00000683409.1:n.1702A=
ENST00000683459.1:n.3682A=
ENST00000683590.1:c.2897-5520A= ENSP00000506820.1:n.2897-5520A=
ENST00000683623.1:c.3002A= ENSP00000507702.1:p.Glu1001=
ENST00000683645.1:n.3646A=
ENST00000683796.1:c.*2967A= ENSP00000508221.1:n.*2967A=
ENST00000683802.1:n.6020A=
ENST00000683833.1:c.3086A= ENSP00000506852.1:p.Glu1029=
ENST00000683994.1:c.3095A= ENSP00000507181.1:p.Glu1032=
ENST00000684290.1:c.*631A= ENSP00000507243.1:n.*631A=
ENST00000684306.1:c.*3008A= ENSP00000508384.1:n.*3008A=
ENST00000684341.1:n.3115A=
ENST00000684383.1:c.*2733A= ENSP00000506863.1:n.*2733A=
ENST00000684619.1:c.*2967A= ENSP00000508088.1:n.*2967A=
ENST00000684705.1:n.216A=
ENST00000684743.1:n.4126A=
ENST00000260665.12:c.3095A= MANE Select ENSP00000260665.7:p.Glu1032=
ENST00000260665.11:c.3095A= ENSP00000260665.7:p.Glu1032=
NM_133259.3:c.3095A= NP_573566.2:p.Glu1032=
XM_006711915.2:c.3017A= XP_006711978.1:p.Glu1006=
XM_006711916.2:c.3095A= XP_006711979.1:p.Glu1032=
XM_011532473.1:c.3095A= XP_011530775.1:p.Glu1032=
XM_011532474.1:c.3095A= XP_011530776.1:p.Glu1032=
XM_006711916.3:c.3095A= XP_006711979.1:p.Glu1032=
XM_017003117.1:c.3017A= XP_016858606.1:p.Glu1006=
XR_002958896.1:n.3137A=
NM_133259.4:c.3095A= MANE Select NP_573566.2:p.Glu1032=