Canonical Allele Identifier: CA2658833941
Gene: LRPPRC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43894536_43894537del , CM000664.2:g.43894536_43894537del GRCh38
NC_000002.11:g.44121675_44121676del , CM000664.1:g.44121675_44121676del GRCh37
NC_000002.10:g.43975179_43975180del NCBI36
NG_008247.1:g.106469_106470del

Transcript Alleles

HGVS Amino-acid Change
ENST00000419884.6:c.615+8_615+9del
ENST00000681993.1:n.1537+8_1537+9del
ENST00000682154.1:n.1419+8_1419+9del
ENST00000682303.1:c.*3696+8_*3696+9del ENSP00000508325.1:n.*3696+8_*3696+9del
ENST00000682308.1:c.3910+8_3910+9del ENSP00000507056.1:n.3910+8_3910+9del
ENST00000682434.1:n.3540+8_3540+9del
ENST00000682480.1:c.4003+8_4003+9del ENSP00000508344.1:n.4003+8_4003+9del
ENST00000682546.1:c.3982+8_3982+9del ENSP00000508188.1:n.3982+8_3982+9del
ENST00000682585.1:c.*113+8_*113+9del ENSP00000506885.1:n.*113+8_*113+9del
ENST00000682607.1:c.2728+8_2728+9del
ENST00000682612.1:c.752+2097_752+2098del
ENST00000682696.1:c.85+8_85+9del ENSP00000508411.1:n.85+8_85+9del
ENST00000682779.1:c.3976+8_3976+9del ENSP00000507947.1:n.3976+8_3976+9del
ENST00000682885.1:c.3940+8_3940+9del ENSP00000508036.1:n.3940+8_3940+9del
ENST00000682933.1:n.4185+8_4185+9del
ENST00000683002.1:c.837+8_837+9del
ENST00000683072.1:n.4569+8_4569+9del
ENST00000683080.1:n.1604+8_1604+9del
ENST00000683096.1:n.2426+8_2426+9del
ENST00000683125.1:c.4093+8_4093+9del ENSP00000507939.1:n.4093+8_4093+9del
ENST00000683213.1:c.3988+8_3988+9del ENSP00000507751.1:n.3988+8_3988+9del
ENST00000683220.1:c.4015+8_4015+9del ENSP00000507151.1:n.4015+8_4015+9del
ENST00000683329.1:n.4788+8_4788+9del
ENST00000683346.1:c.*3860+8_*3860+9del ENSP00000507458.1:n.*3860+8_*3860+9del
ENST00000683409.1:n.2517+8_2517+9del
ENST00000683459.1:n.4572+8_4572+9del
ENST00000683590.1:c.3658+8_3658+9del ENSP00000506820.1:n.3658+8_3658+9del
ENST00000683623.1:c.3892+8_3892+9del ENSP00000507702.1:n.3892+8_3892+9del
ENST00000683796.1:c.*3782+8_*3782+9del ENSP00000508221.1:n.*3782+8_*3782+9del
ENST00000683833.1:c.3901+8_3901+9del ENSP00000506852.1:n.3901+8_3901+9del
ENST00000683994.1:c.*98+8_*98+9del ENSP00000507181.1:n.*98+8_*98+9del
ENST00000684290.1:c.*1446+8_*1446+9del ENSP00000507243.1:n.*1446+8_*1446+9del
ENST00000684306.1:c.*3898+8_*3898+9del ENSP00000508384.1:n.*3898+8_*3898+9del
ENST00000684383.1:c.*3623+8_*3623+9del ENSP00000506863.1:n.*3623+8_*3623+9del
ENST00000684418.1:n.5166+8_5166+9del
ENST00000684433.1:n.369+8_369+9del
ENST00000684454.1:n.7849+8_7849+9del
ENST00000684619.1:c.*3857+8_*3857+9del ENSP00000508088.1:n.*3857+8_*3857+9del
ENST00000684743.1:n.6730+8_6730+9del
ENST00000260665.12:c.3985+8_3985+9del MANE Select ENSP00000260665.7:n.3985+8_3985+9del
ENST00000260665.11:c.3985+8_3985+9del ENSP00000260665.7:n.3985+8_3985+9del
ENST00000419884.5:c.226+8_226+9del ENSP00000414207.1:n.226+8_226+9del
ENST00000463456.5:n.3028+8_3028+9del
NM_133259.3:c.3985+8_3985+9del NP_573566.2:n.3985+8_3985+9del
XM_006711915.2:c.3907+8_3907+9del XP_006711978.1:n.3907+8_3907+9del
XM_011532473.1:c.3910+8_3910+9del XP_011530775.1:n.3910+8_3910+9del
XM_011532474.1:c.3985+8_3985+9del XP_011530776.1:n.3985+8_3985+9del
XM_017003117.1:c.3832+8_3832+9del XP_016858606.1:n.3832+8_3832+9del
XR_002958896.1:n.4027+8_4027+9del
NM_133259.4:c.3985+8_3985+9del MANE Select NP_573566.2:n.3985+8_3985+9del