Canonical Allele Identifier: CA2493977931
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43899262A= , CM000664.2:g.43899262A= GRCh38
NC_000002.11:g.44126401A= , CM000664.1:g.44126401A= GRCh37
NC_000002.10:g.43979905A= NCBI36
NG_008247.1:g.101744T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000419884.6:c.213T=
ENST00000472420.6:n.861T=
ENST00000483489.2:n.213T=
ENST00000681993.1:n.1334T=
ENST00000682303.1:c.*3568T= ENSP00000508325.1:n.*3568T=
ENST00000682308.1:c.3782T= ENSP00000507056.1:p.Leu1261=
ENST00000682434.1:n.1333T=
ENST00000682480.1:c.3800T= ENSP00000508344.1:p.Leu1267=
ENST00000682546.1:c.3779T= ENSP00000508188.1:p.Leu1260=
ENST00000682585.1:c.3782T= ENSP00000506885.1:p.Leu1261=
ENST00000682595.1:n.4366T=
ENST00000682607.1:c.2200T=
ENST00000682612.1:c.634T=
ENST00000682779.1:c.3773T= ENSP00000507947.1:p.Leu1258=
ENST00000682845.1:n.2884T=
ENST00000682885.1:c.3737T= ENSP00000508036.1:p.Leu1246=
ENST00000682933.1:n.3856T=
ENST00000683002.1:c.634T=
ENST00000683072.1:n.4366T=
ENST00000683080.1:n.1401T=
ENST00000683125.1:c.3890T= ENSP00000507939.1:p.Leu1297=
ENST00000683213.1:c.3785T= ENSP00000507751.1:p.Leu1262=
ENST00000683220.1:c.3812T= ENSP00000507151.1:p.Leu1271=
ENST00000683329.1:n.4585T=
ENST00000683346.1:c.*3657T= ENSP00000507458.1:n.*3657T=
ENST00000683409.1:n.2389T=
ENST00000683459.1:n.4369T=
ENST00000683528.1:c.710T=
ENST00000683590.1:c.3530T= ENSP00000506820.1:p.Leu1177=
ENST00000683623.1:c.3689T= ENSP00000507702.1:p.Leu1230=
ENST00000683645.1:n.4333T=
ENST00000683796.1:c.*3654T= ENSP00000508221.1:n.*3654T=
ENST00000683802.1:n.6707T=
ENST00000683833.1:c.3773T= ENSP00000506852.1:p.Leu1258=
ENST00000683994.1:c.3782T= ENSP00000507181.1:p.Leu1261=
ENST00000684290.1:c.*1318T= ENSP00000507243.1:n.*1318T=
ENST00000684306.1:c.*3695T= ENSP00000508384.1:n.*3695T=
ENST00000684341.1:n.3802T=
ENST00000684383.1:c.*3420T= ENSP00000506863.1:n.*3420T=
ENST00000684418.1:n.4963T=
ENST00000684433.1:n.166T=
ENST00000684454.1:n.3132T=
ENST00000684619.1:c.*3654T= ENSP00000508088.1:n.*3654T=
ENST00000684743.1:n.6527T=
ENST00000260665.12:c.3782T= MANE Select ENSP00000260665.7:p.Leu1261=
ENST00000260665.11:c.3782T= ENSP00000260665.7:p.Leu1261=
ENST00000419884.5:c.23T= ENSP00000414207.1:p.Leu8=
ENST00000463456.5:n.2825T=
ENST00000472420.5:n.179T=
ENST00000483489.1:n.256T=
NM_133259.3:c.3782T= NP_573566.2:p.Leu1261=
XM_006711915.2:c.3704T= XP_006711978.1:p.Leu1235=
XM_011532473.1:c.3782T= XP_011530775.1:p.Leu1261=
XM_011532474.1:c.3782T= XP_011530776.1:p.Leu1261=
XM_017003117.1:c.3704T= XP_016858606.1:p.Leu1235=
XR_002958896.1:n.3824T=
NM_133259.4:c.3782T= MANE Select NP_573566.2:p.Leu1261=