Canonical Allele Identifier: CA2493977926
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43899248T= , CM000664.2:g.43899248T= GRCh38
NC_000002.11:g.44126387T= , CM000664.1:g.44126387T= GRCh37
NC_000002.10:g.43979891T= NCBI36
NG_008247.1:g.101758A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000419884.6:c.227A=
ENST00000472420.6:n.875A=
ENST00000483489.2:n.227A=
ENST00000681993.1:n.1348A=
ENST00000682303.1:c.*3582A= ENSP00000508325.1:n.*3582A=
ENST00000682308.1:c.3796A= ENSP00000507056.1:p.Lys1266=
ENST00000682434.1:n.1347A=
ENST00000682480.1:c.3814A= ENSP00000508344.1:p.Lys1272=
ENST00000682546.1:c.3793A= ENSP00000508188.1:p.Lys1265=
ENST00000682585.1:c.3796A= ENSP00000506885.1:p.Lys1266=
ENST00000682595.1:n.4380A=
ENST00000682607.1:c.2214A=
ENST00000682612.1:c.648A=
ENST00000682779.1:c.3787A= ENSP00000507947.1:p.Lys1263=
ENST00000682845.1:n.2898A=
ENST00000682885.1:c.3751A= ENSP00000508036.1:p.Lys1251=
ENST00000682933.1:n.3870A=
ENST00000683002.1:c.648A=
ENST00000683072.1:n.4380A=
ENST00000683080.1:n.1415A=
ENST00000683125.1:c.3904A= ENSP00000507939.1:p.Lys1302=
ENST00000683213.1:c.3799A= ENSP00000507751.1:p.Lys1267=
ENST00000683220.1:c.3826A= ENSP00000507151.1:p.Lys1276=
ENST00000683329.1:n.4599A=
ENST00000683346.1:c.*3671A= ENSP00000507458.1:n.*3671A=
ENST00000683409.1:n.2403A=
ENST00000683459.1:n.4383A=
ENST00000683528.1:c.724A=
ENST00000683590.1:c.3544A= ENSP00000506820.1:p.Lys1182=
ENST00000683623.1:c.3703A= ENSP00000507702.1:p.Lys1235=
ENST00000683645.1:n.4347A=
ENST00000683796.1:c.*3668A= ENSP00000508221.1:n.*3668A=
ENST00000683802.1:n.6721A=
ENST00000683833.1:c.3787A= ENSP00000506852.1:p.Lys1263=
ENST00000683994.1:c.3796A= ENSP00000507181.1:p.Lys1266=
ENST00000684290.1:c.*1332A= ENSP00000507243.1:n.*1332A=
ENST00000684306.1:c.*3709A= ENSP00000508384.1:n.*3709A=
ENST00000684341.1:n.3816A=
ENST00000684383.1:c.*3434A= ENSP00000506863.1:n.*3434A=
ENST00000684418.1:n.4977A=
ENST00000684433.1:n.180A=
ENST00000684454.1:n.3146A=
ENST00000684619.1:c.*3668A= ENSP00000508088.1:n.*3668A=
ENST00000684743.1:n.6541A=
ENST00000260665.12:c.3796A= MANE Select ENSP00000260665.7:p.Lys1266=
ENST00000260665.11:c.3796A= ENSP00000260665.7:p.Lys1266=
ENST00000419884.5:c.37A= ENSP00000414207.1:p.Lys13=
ENST00000463456.5:n.2839A=
ENST00000472420.5:n.193A=
ENST00000483489.1:n.270A=
NM_133259.3:c.3796A= NP_573566.2:p.Lys1266=
XM_006711915.2:c.3718A= XP_006711978.1:p.Lys1240=
XM_011532473.1:c.3796A= XP_011530775.1:p.Lys1266=
XM_011532474.1:c.3796A= XP_011530776.1:p.Lys1266=
XM_017003117.1:c.3718A= XP_016858606.1:p.Lys1240=
XR_002958896.1:n.3838A=
NM_133259.4:c.3796A= MANE Select NP_573566.2:p.Lys1266=