Canonical Allele Identifier: CA2493988109
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43918087G= , CM000664.2:g.43918087G= GRCh38
NC_000002.11:g.44145226G= , CM000664.1:g.44145226G= GRCh37
NC_000002.10:g.43998730G= NCBI36
NG_008247.1:g.82919C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681993.1:n.638C=
ENST00000682295.1:c.303+169C= ENSP00000507499.1:n.303+169C=
ENST00000682303.1:c.*2872C= ENSP00000508325.1:n.*2872C=
ENST00000682308.1:c.3086C= ENSP00000507056.1:p.Ser1029=
ENST00000682480.1:c.3104C= ENSP00000508344.1:p.Ser1035=
ENST00000682546.1:c.3083C= ENSP00000508188.1:p.Ser1028=
ENST00000682585.1:c.3086C= ENSP00000506885.1:p.Ser1029=
ENST00000682595.1:n.3670C=
ENST00000682607.1:c.1504C=
ENST00000682779.1:c.3077C= ENSP00000507947.1:p.Ser1026=
ENST00000682845.1:n.2188C=
ENST00000682885.1:c.3041C= ENSP00000508036.1:p.Ser1014=
ENST00000682933.1:n.3160C=
ENST00000683072.1:n.3670C=
ENST00000683080.1:n.705C=
ENST00000683125.1:c.3194C= ENSP00000507939.1:p.Ser1065=
ENST00000683213.1:c.3089C= ENSP00000507751.1:p.Ser1030=
ENST00000683220.1:c.3116C= ENSP00000507151.1:p.Ser1039=
ENST00000683329.1:n.3889C=
ENST00000683346.1:c.*2961C= ENSP00000507458.1:n.*2961C=
ENST00000683409.1:n.1693C=
ENST00000683459.1:n.3673C=
ENST00000683590.1:c.2897-5529C= ENSP00000506820.1:n.2897-5529C=
ENST00000683623.1:c.2993C= ENSP00000507702.1:p.Ser998=
ENST00000683645.1:n.3637C=
ENST00000683796.1:c.*2958C= ENSP00000508221.1:n.*2958C=
ENST00000683802.1:n.6011C=
ENST00000683833.1:c.3077C= ENSP00000506852.1:p.Ser1026=
ENST00000683994.1:c.3086C= ENSP00000507181.1:p.Ser1029=
ENST00000684290.1:c.*622C= ENSP00000507243.1:n.*622C=
ENST00000684306.1:c.*2999C= ENSP00000508384.1:n.*2999C=
ENST00000684341.1:n.3106C=
ENST00000684383.1:c.*2724C= ENSP00000506863.1:n.*2724C=
ENST00000684619.1:c.*2958C= ENSP00000508088.1:n.*2958C=
ENST00000684705.1:n.207C=
ENST00000684743.1:n.4117C=
ENST00000260665.12:c.3086C= MANE Select ENSP00000260665.7:p.Ser1029=
ENST00000260665.11:c.3086C= ENSP00000260665.7:p.Ser1029=
NM_133259.3:c.3086C= NP_573566.2:p.Ser1029=
XM_006711915.2:c.3008C= XP_006711978.1:p.Ser1003=
XM_006711916.2:c.3086C= XP_006711979.1:p.Ser1029=
XM_011532473.1:c.3086C= XP_011530775.1:p.Ser1029=
XM_011532474.1:c.3086C= XP_011530776.1:p.Ser1029=
XM_006711916.3:c.3086C= XP_006711979.1:p.Ser1029=
XM_017003117.1:c.3008C= XP_016858606.1:p.Ser1003=
XR_002958896.1:n.3128C=
NM_133259.4:c.3086C= MANE Select NP_573566.2:p.Ser1029=