Canonical Allele Identifier: CA2493975281
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43894629C= , CM000664.2:g.43894629C= GRCh38
NC_000002.11:g.44121768C= , CM000664.1:g.44121768C= GRCh37
NC_000002.10:g.43975272C= NCBI36
NG_008247.1:g.106377G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000419884.6:c.531G=
ENST00000681993.1:n.1453G=
ENST00000682154.1:n.1335G=
ENST00000682303.1:c.*3612G= ENSP00000508325.1:n.*3612G=
ENST00000682308.1:c.3826G= ENSP00000507056.1:p.Ala1276=
ENST00000682434.1:n.3456G=
ENST00000682480.1:c.3919G= ENSP00000508344.1:p.Ala1307=
ENST00000682546.1:c.3898G= ENSP00000508188.1:p.Ala1300=
ENST00000682585.1:c.*29G= ENSP00000506885.1:n.*29G=
ENST00000682607.1:c.2644G=
ENST00000682612.1:c.752+2005G=
ENST00000682696.1:c.1G= ENSP00000508411.1:p.Ala1=
ENST00000682779.1:c.3892G= ENSP00000507947.1:p.Ala1298=
ENST00000682885.1:c.3856G= ENSP00000508036.1:p.Ala1286=
ENST00000682933.1:n.4101G=
ENST00000683002.1:c.753G=
ENST00000683072.1:n.4485G=
ENST00000683080.1:n.1520G=
ENST00000683096.1:n.2342G=
ENST00000683125.1:c.4009G= ENSP00000507939.1:p.Ala1337=
ENST00000683213.1:c.3904G= ENSP00000507751.1:p.Ala1302=
ENST00000683220.1:c.3931G= ENSP00000507151.1:p.Ala1311=
ENST00000683329.1:n.4704G=
ENST00000683346.1:c.*3776G= ENSP00000507458.1:n.*3776G=
ENST00000683409.1:n.2433G=
ENST00000683459.1:n.4488G=
ENST00000683590.1:c.3574G= ENSP00000506820.1:p.Ala1192=
ENST00000683623.1:c.3808G= ENSP00000507702.1:p.Ala1270=
ENST00000683796.1:c.*3698G= ENSP00000508221.1:n.*3698G=
ENST00000683833.1:c.3817G= ENSP00000506852.1:p.Ala1273=
ENST00000683994.1:c.*14G= ENSP00000507181.1:n.*14G=
ENST00000684290.1:c.*1362G= ENSP00000507243.1:n.*1362G=
ENST00000684306.1:c.*3814G= ENSP00000508384.1:n.*3814G=
ENST00000684383.1:c.*3539G= ENSP00000506863.1:n.*3539G=
ENST00000684418.1:n.5082G=
ENST00000684433.1:n.285G=
ENST00000684454.1:n.7765G=
ENST00000684619.1:c.*3773G= ENSP00000508088.1:n.*3773G=
ENST00000684743.1:n.6646G=
ENST00000260665.12:c.3901G= MANE Select ENSP00000260665.7:p.Ala1301=
ENST00000260665.11:c.3901G= ENSP00000260665.7:p.Ala1301=
ENST00000419884.5:c.142G= ENSP00000414207.1:p.Ala48=
ENST00000463456.5:n.2944G=
NM_133259.3:c.3901G= NP_573566.2:p.Ala1301=
XM_006711915.2:c.3823G= XP_006711978.1:p.Ala1275=
XM_011532473.1:c.3826G= XP_011530775.1:p.Ala1276=
XM_011532474.1:c.3901G= XP_011530776.1:p.Ala1301=
XM_017003117.1:c.3748G= XP_016858606.1:p.Ala1250=
XR_002958896.1:n.3943G=
NM_133259.4:c.3901G= MANE Select NP_573566.2:p.Ala1301=