Canonical Allele Identifier: CA2493977915
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43899222T= , CM000664.2:g.43899222T= GRCh38
NC_000002.11:g.44126361T= , CM000664.1:g.44126361T= GRCh37
NC_000002.10:g.43979865T= NCBI36
NG_008247.1:g.101784A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000419884.6:c.253A=
ENST00000472420.6:n.901A=
ENST00000483489.2:n.253A=
ENST00000681993.1:n.1374A=
ENST00000682303.1:c.*3608A= ENSP00000508325.1:n.*3608A=
ENST00000682308.1:c.3822A= ENSP00000507056.1:p.Leu1274=
ENST00000682434.1:n.1373A=
ENST00000682480.1:c.3840A= ENSP00000508344.1:p.Leu1280=
ENST00000682546.1:c.3819A= ENSP00000508188.1:p.Leu1273=
ENST00000682585.1:c.3822A= ENSP00000506885.1:p.Leu1274=
ENST00000682595.1:n.4406A=
ENST00000682607.1:c.2240A=
ENST00000682612.1:c.674A=
ENST00000682779.1:c.3813A= ENSP00000507947.1:p.Leu1271=
ENST00000682885.1:c.3777A= ENSP00000508036.1:p.Leu1259=
ENST00000682933.1:n.3896A=
ENST00000683002.1:c.674A=
ENST00000683072.1:n.4406A=
ENST00000683080.1:n.1441A=
ENST00000683125.1:c.3930A= ENSP00000507939.1:p.Leu1310=
ENST00000683213.1:c.3825A= ENSP00000507751.1:p.Leu1275=
ENST00000683220.1:c.3852A= ENSP00000507151.1:p.Leu1284=
ENST00000683329.1:n.4625A=
ENST00000683346.1:c.*3697A= ENSP00000507458.1:n.*3697A=
ENST00000683409.1:n.2429A=
ENST00000683459.1:n.4409A=
ENST00000683528.1:c.750A=
ENST00000683590.1:c.3570A= ENSP00000506820.1:p.Leu1190=
ENST00000683623.1:c.3729A= ENSP00000507702.1:p.Leu1243=
ENST00000683645.1:n.4373A=
ENST00000683796.1:c.*3694A= ENSP00000508221.1:n.*3694A=
ENST00000683833.1:c.3813A= ENSP00000506852.1:p.Leu1271=
ENST00000683994.1:c.3822A= ENSP00000507181.1:p.Leu1274=
ENST00000684290.1:c.*1358A= ENSP00000507243.1:n.*1358A=
ENST00000684306.1:c.*3735A= ENSP00000508384.1:n.*3735A=
ENST00000684341.1:n.3842A=
ENST00000684383.1:c.*3460A= ENSP00000506863.1:n.*3460A=
ENST00000684418.1:n.5003A=
ENST00000684433.1:n.206A=
ENST00000684454.1:n.3172A=
ENST00000684619.1:c.*3694A= ENSP00000508088.1:n.*3694A=
ENST00000684743.1:n.6567A=
ENST00000260665.12:c.3822A= MANE Select ENSP00000260665.7:p.Leu1274=
ENST00000260665.11:c.3822A= ENSP00000260665.7:p.Leu1274=
ENST00000419884.5:c.63A= ENSP00000414207.1:p.Leu21=
ENST00000463456.5:n.2865A=
ENST00000472420.5:n.219A=
ENST00000483489.1:n.296A=
NM_133259.3:c.3822A= NP_573566.2:p.Leu1274=
XM_006711915.2:c.3744A= XP_006711978.1:p.Leu1248=
XM_011532473.1:c.3822A= XP_011530775.1:p.Leu1274=
XM_011532474.1:c.3822A= XP_011530776.1:p.Leu1274=
XM_017003117.1:c.3744A= XP_016858606.1:p.Leu1248=
XR_002958896.1:n.3864A=
NM_133259.4:c.3822A= MANE Select NP_573566.2:p.Leu1274=