Canonical Allele Identifier: CA2576954008
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43894495_43894498del , CM000664.2:g.43894495_43894498del GRCh38
NC_000002.11:g.44121634_44121637del , CM000664.1:g.44121634_44121637del GRCh37
NC_000002.10:g.43975138_43975141del NCBI36
NG_008247.1:g.106511_106514del

Transcript Alleles

HGVS Amino-acid Change
ENST00000419884.6:c.615+50_615+53del
ENST00000681993.1:n.1537+50_1537+53del
ENST00000682154.1:n.1419+50_1419+53del
ENST00000682303.1:c.*3696+50_*3696+53del ENSP00000508325.1:n.*3696+50_*3696+53del
ENST00000682308.1:c.3910+50_3910+53del ENSP00000507056.1:n.3910+50_3910+53del
ENST00000682434.1:n.3540+50_3540+53del
ENST00000682480.1:c.4003+50_4003+53del ENSP00000508344.1:n.4003+50_4003+53del
ENST00000682546.1:c.3982+50_3982+53del ENSP00000508188.1:n.3982+50_3982+53del
ENST00000682585.1:c.*113+50_*113+53del ENSP00000506885.1:n.*113+50_*113+53del
ENST00000682607.1:c.2728+50_2728+53del
ENST00000682612.1:c.752+2139_752+2142del
ENST00000682696.1:c.85+50_85+53del ENSP00000508411.1:n.85+50_85+53del
ENST00000682779.1:c.3976+50_3976+53del ENSP00000507947.1:n.3976+50_3976+53del
ENST00000682885.1:c.3940+50_3940+53del ENSP00000508036.1:n.3940+50_3940+53del
ENST00000682933.1:n.4185+50_4185+53del
ENST00000683002.1:c.837+50_837+53del
ENST00000683072.1:n.4569+50_4569+53del
ENST00000683080.1:n.1604+50_1604+53del
ENST00000683096.1:n.2426+50_2426+53del
ENST00000683125.1:c.4093+50_4093+53del ENSP00000507939.1:n.4093+50_4093+53del
ENST00000683213.1:c.3988+50_3988+53del ENSP00000507751.1:n.3988+50_3988+53del
ENST00000683220.1:c.4015+50_4015+53del ENSP00000507151.1:n.4015+50_4015+53del
ENST00000683329.1:n.4788+50_4788+53del
ENST00000683346.1:c.*3860+50_*3860+53del ENSP00000507458.1:n.*3860+50_*3860+53del
ENST00000683409.1:n.2517+50_2517+53del
ENST00000683459.1:n.4572+50_4572+53del
ENST00000683590.1:c.3658+50_3658+53del ENSP00000506820.1:n.3658+50_3658+53del
ENST00000683623.1:c.3892+50_3892+53del ENSP00000507702.1:n.3892+50_3892+53del
ENST00000683796.1:c.*3782+50_*3782+53del ENSP00000508221.1:n.*3782+50_*3782+53del
ENST00000683833.1:c.3901+50_3901+53del ENSP00000506852.1:n.3901+50_3901+53del
ENST00000683994.1:c.*98+50_*98+53del ENSP00000507181.1:n.*98+50_*98+53del
ENST00000684290.1:c.*1446+50_*1446+53del ENSP00000507243.1:n.*1446+50_*1446+53del
ENST00000684306.1:c.*3898+50_*3898+53del ENSP00000508384.1:n.*3898+50_*3898+53del
ENST00000684383.1:c.*3623+50_*3623+53del ENSP00000506863.1:n.*3623+50_*3623+53del
ENST00000684418.1:n.5166+50_5166+53del
ENST00000684433.1:n.369+50_369+53del
ENST00000684454.1:n.7849+50_7849+53del
ENST00000684619.1:c.*3857+50_*3857+53del ENSP00000508088.1:n.*3857+50_*3857+53del
ENST00000684743.1:n.6730+50_6730+53del
ENST00000260665.12:c.3985+50_3985+53del MANE Select ENSP00000260665.7:n.3985+50_3985+53del
ENST00000260665.11:c.3985+50_3985+53del ENSP00000260665.7:n.3985+50_3985+53del
ENST00000419884.5:c.226+50_226+53del ENSP00000414207.1:n.226+50_226+53del
ENST00000463456.5:n.3028+50_3028+53del
NM_133259.3:c.3985+50_3985+53del NP_573566.2:n.3985+50_3985+53del
XM_006711915.2:c.3907+50_3907+53del XP_006711978.1:n.3907+50_3907+53del
XM_011532473.1:c.3910+50_3910+53del XP_011530775.1:n.3910+50_3910+53del
XM_011532474.1:c.3985+50_3985+53del XP_011530776.1:n.3985+50_3985+53del
XM_017003117.1:c.3832+50_3832+53del XP_016858606.1:n.3832+50_3832+53del
XR_002958896.1:n.4027+50_4027+53del
NM_133259.4:c.3985+50_3985+53del MANE Select NP_573566.2:n.3985+50_3985+53del