Canonical Allele Identifier: CA2493981270
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43905769T= , CM000664.2:g.43905769T= GRCh38
NC_000002.11:g.44132908T= , CM000664.1:g.44132908T= GRCh37
NC_000002.10:g.43986412T= NCBI36
NG_008247.1:g.95237A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000472420.6:n.366A=
ENST00000681993.1:n.839A=
ENST00000682295.1:c.442A= ENSP00000507499.1:n.442A=
ENST00000682303.1:c.*3073A= ENSP00000508325.1:n.*3073A=
ENST00000682308.1:c.3287A= ENSP00000507056.1:p.His1096=
ENST00000682480.1:c.3305A= ENSP00000508344.1:p.His1102=
ENST00000682546.1:c.3284A= ENSP00000508188.1:p.His1095=
ENST00000682585.1:c.3287A= ENSP00000506885.1:p.His1096=
ENST00000682595.1:n.3871A=
ENST00000682607.1:c.1705A=
ENST00000682612.1:c.139A=
ENST00000682779.1:c.3278A= ENSP00000507947.1:p.His1093=
ENST00000682845.1:n.2389A=
ENST00000682885.1:c.3242A= ENSP00000508036.1:p.His1081=
ENST00000682933.1:n.3361A=
ENST00000683002.1:c.139A=
ENST00000683072.1:n.3871A=
ENST00000683080.1:n.906A=
ENST00000683125.1:c.3395A= ENSP00000507939.1:p.His1132=
ENST00000683213.1:c.3290A= ENSP00000507751.1:p.His1097=
ENST00000683220.1:c.3317A= ENSP00000507151.1:p.His1106=
ENST00000683329.1:n.4090A=
ENST00000683346.1:c.*3162A= ENSP00000507458.1:n.*3162A=
ENST00000683409.1:n.1894A=
ENST00000683459.1:n.3874A=
ENST00000683528.1:c.139A=
ENST00000683590.1:c.3035A= ENSP00000506820.1:p.His1012=
ENST00000683623.1:c.3194A= ENSP00000507702.1:p.His1065=
ENST00000683645.1:n.3838A=
ENST00000683796.1:c.*3159A= ENSP00000508221.1:n.*3159A=
ENST00000683802.1:n.6212A=
ENST00000683833.1:c.3278A= ENSP00000506852.1:p.His1093=
ENST00000683994.1:c.3287A= ENSP00000507181.1:p.His1096=
ENST00000684290.1:c.*823A= ENSP00000507243.1:n.*823A=
ENST00000684306.1:c.*3200A= ENSP00000508384.1:n.*3200A=
ENST00000684341.1:n.3307A=
ENST00000684383.1:c.*2925A= ENSP00000506863.1:n.*2925A=
ENST00000684418.1:n.4468A=
ENST00000684454.1:n.2637A=
ENST00000684619.1:c.*3159A= ENSP00000508088.1:n.*3159A=
ENST00000684743.1:n.4318A=
ENST00000260665.12:c.3287A= MANE Select ENSP00000260665.7:p.His1096=
ENST00000260665.11:c.3287A= ENSP00000260665.7:p.His1096=
NM_133259.3:c.3287A= NP_573566.2:p.His1096=
XM_006711915.2:c.3209A= XP_006711978.1:p.His1070=
XM_011532473.1:c.3287A= XP_011530775.1:p.His1096=
XM_011532474.1:c.3287A= XP_011530776.1:p.His1096=
XM_017003117.1:c.3209A= XP_016858606.1:p.His1070=
XR_002958896.1:n.3329A=
NM_133259.4:c.3287A= MANE Select NP_573566.2:p.His1096=