Canonical Allele Identifier: CA2493975252
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43894551T= , CM000664.2:g.43894551T= GRCh38
NC_000002.11:g.44121690T= , CM000664.1:g.44121690T= GRCh37
NC_000002.10:g.43975194T= NCBI36
NG_008247.1:g.106455A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000419884.6:c.609A=
ENST00000681993.1:n.1531A=
ENST00000682154.1:n.1413A=
ENST00000682303.1:c.*3690A= ENSP00000508325.1:n.*3690A=
ENST00000682308.1:c.3904A= ENSP00000507056.1:p.Ser1302=
ENST00000682434.1:n.3534A=
ENST00000682480.1:c.3997A= ENSP00000508344.1:p.Ser1333=
ENST00000682546.1:c.3976A= ENSP00000508188.1:p.Ser1326=
ENST00000682585.1:c.*107A= ENSP00000506885.1:n.*107A=
ENST00000682607.1:c.2722A=
ENST00000682612.1:c.752+2083A=
ENST00000682696.1:c.79A= ENSP00000508411.1:p.Ser27=
ENST00000682779.1:c.3970A= ENSP00000507947.1:p.Ser1324=
ENST00000682885.1:c.3934A= ENSP00000508036.1:p.Ser1312=
ENST00000682933.1:n.4179A=
ENST00000683002.1:c.831A=
ENST00000683072.1:n.4563A=
ENST00000683080.1:n.1598A=
ENST00000683096.1:n.2420A=
ENST00000683125.1:c.4087A= ENSP00000507939.1:p.Ser1363=
ENST00000683213.1:c.3982A= ENSP00000507751.1:p.Ser1328=
ENST00000683220.1:c.4009A= ENSP00000507151.1:p.Ser1337=
ENST00000683329.1:n.4782A=
ENST00000683346.1:c.*3854A= ENSP00000507458.1:n.*3854A=
ENST00000683409.1:n.2511A=
ENST00000683459.1:n.4566A=
ENST00000683590.1:c.3652A= ENSP00000506820.1:p.Ser1218=
ENST00000683623.1:c.3886A= ENSP00000507702.1:p.Ser1296=
ENST00000683796.1:c.*3776A= ENSP00000508221.1:n.*3776A=
ENST00000683833.1:c.3895A= ENSP00000506852.1:p.Ser1299=
ENST00000683994.1:c.*92A= ENSP00000507181.1:n.*92A=
ENST00000684290.1:c.*1440A= ENSP00000507243.1:n.*1440A=
ENST00000684306.1:c.*3892A= ENSP00000508384.1:n.*3892A=
ENST00000684383.1:c.*3617A= ENSP00000506863.1:n.*3617A=
ENST00000684418.1:n.5160A=
ENST00000684433.1:n.363A=
ENST00000684454.1:n.7843A=
ENST00000684619.1:c.*3851A= ENSP00000508088.1:n.*3851A=
ENST00000684743.1:n.6724A=
ENST00000260665.12:c.3979A= MANE Select ENSP00000260665.7:p.Ser1327=
ENST00000260665.11:c.3979A= ENSP00000260665.7:p.Ser1327=
ENST00000419884.5:c.220A= ENSP00000414207.1:p.Ser74=
ENST00000463456.5:n.3022A=
NM_133259.3:c.3979A= NP_573566.2:p.Ser1327=
XM_006711915.2:c.3901A= XP_006711978.1:p.Ser1301=
XM_011532473.1:c.3904A= XP_011530775.1:p.Ser1302=
XM_011532474.1:c.3979A= XP_011530776.1:p.Ser1327=
XM_017003117.1:c.3826A= XP_016858606.1:p.Ser1276=
XR_002958896.1:n.4021A=
NM_133259.4:c.3979A= MANE Select NP_573566.2:p.Ser1327=