Canonical Allele Identifier: CA2493981271
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43905770G= , CM000664.2:g.43905770G= GRCh38
NC_000002.11:g.44132909G= , CM000664.1:g.44132909G= GRCh37
NC_000002.10:g.43986413G= NCBI36
NG_008247.1:g.95236C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000472420.6:n.365C=
ENST00000681993.1:n.838C=
ENST00000682295.1:c.441C= ENSP00000507499.1:n.441C=
ENST00000682303.1:c.*3072C= ENSP00000508325.1:n.*3072C=
ENST00000682308.1:c.3286C= ENSP00000507056.1:p.His1096=
ENST00000682480.1:c.3304C= ENSP00000508344.1:p.His1102=
ENST00000682546.1:c.3283C= ENSP00000508188.1:p.His1095=
ENST00000682585.1:c.3286C= ENSP00000506885.1:p.His1096=
ENST00000682595.1:n.3870C=
ENST00000682607.1:c.1704C=
ENST00000682612.1:c.138C=
ENST00000682779.1:c.3277C= ENSP00000507947.1:p.His1093=
ENST00000682845.1:n.2388C=
ENST00000682885.1:c.3241C= ENSP00000508036.1:p.His1081=
ENST00000682933.1:n.3360C=
ENST00000683002.1:c.138C=
ENST00000683072.1:n.3870C=
ENST00000683080.1:n.905C=
ENST00000683125.1:c.3394C= ENSP00000507939.1:p.His1132=
ENST00000683213.1:c.3289C= ENSP00000507751.1:p.His1097=
ENST00000683220.1:c.3316C= ENSP00000507151.1:p.His1106=
ENST00000683329.1:n.4089C=
ENST00000683346.1:c.*3161C= ENSP00000507458.1:n.*3161C=
ENST00000683409.1:n.1893C=
ENST00000683459.1:n.3873C=
ENST00000683528.1:c.138C=
ENST00000683590.1:c.3034C= ENSP00000506820.1:p.His1012=
ENST00000683623.1:c.3193C= ENSP00000507702.1:p.His1065=
ENST00000683645.1:n.3837C=
ENST00000683796.1:c.*3158C= ENSP00000508221.1:n.*3158C=
ENST00000683802.1:n.6211C=
ENST00000683833.1:c.3277C= ENSP00000506852.1:p.His1093=
ENST00000683994.1:c.3286C= ENSP00000507181.1:p.His1096=
ENST00000684290.1:c.*822C= ENSP00000507243.1:n.*822C=
ENST00000684306.1:c.*3199C= ENSP00000508384.1:n.*3199C=
ENST00000684341.1:n.3306C=
ENST00000684383.1:c.*2924C= ENSP00000506863.1:n.*2924C=
ENST00000684418.1:n.4467C=
ENST00000684454.1:n.2636C=
ENST00000684619.1:c.*3158C= ENSP00000508088.1:n.*3158C=
ENST00000684743.1:n.4317C=
ENST00000260665.12:c.3286C= MANE Select ENSP00000260665.7:p.His1096=
ENST00000260665.11:c.3286C= ENSP00000260665.7:p.His1096=
NM_133259.3:c.3286C= NP_573566.2:p.His1096=
XM_006711915.2:c.3208C= XP_006711978.1:p.His1070=
XM_011532473.1:c.3286C= XP_011530775.1:p.His1096=
XM_011532474.1:c.3286C= XP_011530776.1:p.His1096=
XM_017003117.1:c.3208C= XP_016858606.1:p.His1070=
XR_002958896.1:n.3328C=
NM_133259.4:c.3286C= MANE Select NP_573566.2:p.His1096=