Canonical Allele Identifier: CA2576954533
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43948118_43948121del , CM000664.2:g.43948118_43948121del GRCh38
NC_000002.11:g.44175257_44175260del , CM000664.1:g.44175257_44175260del GRCh37
NC_000002.10:g.44028761_44028764del NCBI36
NG_008247.1:g.52890_52893del

Transcript Alleles

HGVS Amino-acid Change
ENST00000409659.6:c.1920+6_1920+9del ENSP00000386562.2:n.1920+6_1920+9del
ENST00000447246.2:c.1920+6_1920+9del ENSP00000403637.2:n.1920+6_1920+9del
ENST00000681959.1:n.1534+6_1534+9del
ENST00000681961.1:n.1940+6_1940+9del
ENST00000682104.1:c.1794+6_1794+9del ENSP00000507716.1:n.1794+6_1794+9del
ENST00000682303.1:c.*1792+6_*1792+9del ENSP00000508325.1:n.*1792+6_*1792+9del
ENST00000682308.1:c.1920+6_1920+9del ENSP00000507056.1:n.1920+6_1920+9del
ENST00000682480.1:c.1920+6_1920+9del ENSP00000508344.1:n.1920+6_1920+9del
ENST00000682546.1:c.1917+6_1917+9del ENSP00000508188.1:n.1917+6_1917+9del
ENST00000682585.1:c.1920+6_1920+9del ENSP00000506885.1:n.1920+6_1920+9del
ENST00000682595.1:n.2502+6_2502+9del
ENST00000682607.1:c.338+6_338+9del
ENST00000682779.1:c.1911+6_1911+9del ENSP00000507947.1:n.1911+6_1911+9del
ENST00000682885.1:c.1920+6_1920+9del ENSP00000508036.1:n.1920+6_1920+9del
ENST00000682933.1:n.1994+6_1994+9del
ENST00000683072.1:n.2502+6_2502+9del
ENST00000683082.1:n.1944_1947del
ENST00000683125.1:c.1920+6_1920+9del ENSP00000507939.1:n.1920+6_1920+9del
ENST00000683213.1:c.1923+6_1923+9del ENSP00000507751.1:n.1923+6_1923+9del
ENST00000683220.1:c.1950+6_1950+9del ENSP00000507151.1:n.1950+6_1950+9del
ENST00000683329.1:n.2723+6_2723+9del
ENST00000683346.1:c.*1795+6_*1795+9del ENSP00000507458.1:n.*1795+6_*1795+9del
ENST00000683459.1:n.2507+6_2507+9del
ENST00000683590.1:c.1920+6_1920+9del ENSP00000506820.1:n.1920+6_1920+9del
ENST00000683623.1:c.1920+6_1920+9del ENSP00000507702.1:n.1920+6_1920+9del
ENST00000683645.1:n.2471+6_2471+9del
ENST00000683694.1:n.671+6_671+9del
ENST00000683796.1:c.*1792+6_*1792+9del ENSP00000508221.1:n.*1792+6_*1792+9del
ENST00000683802.1:n.4845+6_4845+9del
ENST00000683833.1:c.1911+6_1911+9del ENSP00000506852.1:n.1911+6_1911+9del
ENST00000683934.1:c.1806+6_1806+9del
ENST00000683989.1:c.1920+6_1920+9del ENSP00000507510.1:n.1920+6_1920+9del
ENST00000683994.1:c.1920+6_1920+9del ENSP00000507181.1:n.1920+6_1920+9del
ENST00000684290.1:c.1920+6_1920+9del ENSP00000507243.1:n.1920+6_1920+9del
ENST00000684306.1:c.*1833+6_*1833+9del ENSP00000508384.1:n.*1833+6_*1833+9del
ENST00000684341.1:n.1940+6_1940+9del
ENST00000684383.1:c.*1558+6_*1558+9del ENSP00000506863.1:n.*1558+6_*1558+9del
ENST00000684482.1:c.4389+6_4389+9del
ENST00000684619.1:c.*1792+6_*1792+9del ENSP00000508088.1:n.*1792+6_*1792+9del
ENST00000684743.1:n.2951+6_2951+9del
ENST00000260665.12:c.1920+6_1920+9del MANE Select ENSP00000260665.7:n.1920+6_1920+9del
ENST00000260665.11:c.1920+6_1920+9del ENSP00000260665.7:n.1920+6_1920+9del
NM_133259.3:c.1920+6_1920+9del NP_573566.2:n.1920+6_1920+9del
XM_006711915.2:c.1842+6_1842+9del XP_006711978.1:n.1842+6_1842+9del
XM_006711916.2:c.1920+6_1920+9del XP_006711979.1:n.1920+6_1920+9del
XM_011532473.1:c.1920+6_1920+9del XP_011530775.1:n.1920+6_1920+9del
XM_011532474.1:c.1920+6_1920+9del XP_011530776.1:n.1920+6_1920+9del
XM_006711916.3:c.1920+6_1920+9del XP_006711979.1:n.1920+6_1920+9del
XM_017003117.1:c.1842+6_1842+9del XP_016858606.1:n.1842+6_1842+9del
XR_002958896.1:n.1962+6_1962+9del
NM_133259.4:c.1920+6_1920+9del MANE Select NP_573566.2:n.1920+6_1920+9del