Canonical Allele Identifier: CA2493981235
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43905709C= , CM000664.2:g.43905709C= GRCh38
NC_000002.11:g.44132848C= , CM000664.1:g.44132848C= GRCh37
NC_000002.10:g.43986352C= NCBI36
NG_008247.1:g.95297G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000472420.6:n.426G=
ENST00000681993.1:n.899G=
ENST00000682295.1:c.502G= ENSP00000507499.1:n.502G=
ENST00000682303.1:c.*3133G= ENSP00000508325.1:n.*3133G=
ENST00000682308.1:c.3347G= ENSP00000507056.1:p.Arg1116=
ENST00000682480.1:c.3365G= ENSP00000508344.1:p.Arg1122=
ENST00000682546.1:c.3344G= ENSP00000508188.1:p.Arg1115=
ENST00000682585.1:c.3347G= ENSP00000506885.1:p.Arg1116=
ENST00000682595.1:n.3931G=
ENST00000682607.1:c.1765G=
ENST00000682612.1:c.199G=
ENST00000682779.1:c.3338G= ENSP00000507947.1:p.Arg1113=
ENST00000682845.1:n.2449G=
ENST00000682885.1:c.3302G= ENSP00000508036.1:p.Arg1101=
ENST00000682933.1:n.3421G=
ENST00000683002.1:c.199G=
ENST00000683072.1:n.3931G=
ENST00000683080.1:n.966G=
ENST00000683125.1:c.3455G= ENSP00000507939.1:p.Arg1152=
ENST00000683213.1:c.3350G= ENSP00000507751.1:p.Arg1117=
ENST00000683220.1:c.3377G= ENSP00000507151.1:p.Arg1126=
ENST00000683329.1:n.4150G=
ENST00000683346.1:c.*3222G= ENSP00000507458.1:n.*3222G=
ENST00000683409.1:n.1954G=
ENST00000683459.1:n.3934G=
ENST00000683528.1:c.199G=
ENST00000683590.1:c.3095G= ENSP00000506820.1:p.Arg1032=
ENST00000683623.1:c.3254G= ENSP00000507702.1:p.Arg1085=
ENST00000683645.1:n.3898G=
ENST00000683796.1:c.*3219G= ENSP00000508221.1:n.*3219G=
ENST00000683802.1:n.6272G=
ENST00000683833.1:c.3338G= ENSP00000506852.1:p.Arg1113=
ENST00000683994.1:c.3347G= ENSP00000507181.1:p.Arg1116=
ENST00000684290.1:c.*883G= ENSP00000507243.1:n.*883G=
ENST00000684306.1:c.*3260G= ENSP00000508384.1:n.*3260G=
ENST00000684341.1:n.3367G=
ENST00000684383.1:c.*2985G= ENSP00000506863.1:n.*2985G=
ENST00000684418.1:n.4528G=
ENST00000684454.1:n.2697G=
ENST00000684619.1:c.*3219G= ENSP00000508088.1:n.*3219G=
ENST00000684743.1:n.4378G=
ENST00000260665.12:c.3347G= MANE Select ENSP00000260665.7:p.Arg1116=
ENST00000260665.11:c.3347G= ENSP00000260665.7:p.Arg1116=
NM_133259.3:c.3347G= NP_573566.2:p.Arg1116=
XM_006711915.2:c.3269G= XP_006711978.1:p.Arg1090=
XM_011532473.1:c.3347G= XP_011530775.1:p.Arg1116=
XM_011532474.1:c.3347G= XP_011530776.1:p.Arg1116=
XM_017003117.1:c.3269G= XP_016858606.1:p.Arg1090=
XR_002958896.1:n.3389G=
NM_133259.4:c.3347G= MANE Select NP_573566.2:p.Arg1116=