Canonical Allele Identifier: CA2493981277
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43905779C= , CM000664.2:g.43905779C= GRCh38
NC_000002.11:g.44132918C= , CM000664.1:g.44132918C= GRCh37
NC_000002.10:g.43986422C= NCBI36
NG_008247.1:g.95227G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000472420.6:n.356G=
ENST00000681993.1:n.829G=
ENST00000682295.1:c.432G= ENSP00000507499.1:n.432G=
ENST00000682303.1:c.*3063G= ENSP00000508325.1:n.*3063G=
ENST00000682308.1:c.3277G= ENSP00000507056.1:p.Ala1093=
ENST00000682480.1:c.3295G= ENSP00000508344.1:p.Ala1099=
ENST00000682546.1:c.3274G= ENSP00000508188.1:p.Ala1092=
ENST00000682585.1:c.3277G= ENSP00000506885.1:p.Ala1093=
ENST00000682595.1:n.3861G=
ENST00000682607.1:c.1695G=
ENST00000682612.1:c.129G=
ENST00000682779.1:c.3268G= ENSP00000507947.1:p.Ala1090=
ENST00000682845.1:n.2379G=
ENST00000682885.1:c.3232G= ENSP00000508036.1:p.Ala1078=
ENST00000682933.1:n.3351G=
ENST00000683002.1:c.129G=
ENST00000683072.1:n.3861G=
ENST00000683080.1:n.896G=
ENST00000683125.1:c.3385G= ENSP00000507939.1:p.Ala1129=
ENST00000683213.1:c.3280G= ENSP00000507751.1:p.Ala1094=
ENST00000683220.1:c.3307G= ENSP00000507151.1:p.Ala1103=
ENST00000683329.1:n.4080G=
ENST00000683346.1:c.*3152G= ENSP00000507458.1:n.*3152G=
ENST00000683409.1:n.1884G=
ENST00000683459.1:n.3864G=
ENST00000683528.1:c.129G=
ENST00000683590.1:c.3025G= ENSP00000506820.1:p.Ala1009=
ENST00000683623.1:c.3184G= ENSP00000507702.1:p.Ala1062=
ENST00000683645.1:n.3828G=
ENST00000683796.1:c.*3149G= ENSP00000508221.1:n.*3149G=
ENST00000683802.1:n.6202G=
ENST00000683833.1:c.3268G= ENSP00000506852.1:p.Ala1090=
ENST00000683994.1:c.3277G= ENSP00000507181.1:p.Ala1093=
ENST00000684290.1:c.*813G= ENSP00000507243.1:n.*813G=
ENST00000684306.1:c.*3190G= ENSP00000508384.1:n.*3190G=
ENST00000684341.1:n.3297G=
ENST00000684383.1:c.*2915G= ENSP00000506863.1:n.*2915G=
ENST00000684418.1:n.4458G=
ENST00000684454.1:n.2627G=
ENST00000684619.1:c.*3149G= ENSP00000508088.1:n.*3149G=
ENST00000684743.1:n.4308G=
ENST00000260665.12:c.3277G= MANE Select ENSP00000260665.7:p.Ala1093=
ENST00000260665.11:c.3277G= ENSP00000260665.7:p.Ala1093=
NM_133259.3:c.3277G= NP_573566.2:p.Ala1093=
XM_006711915.2:c.3199G= XP_006711978.1:p.Ala1067=
XM_011532473.1:c.3277G= XP_011530775.1:p.Ala1093=
XM_011532474.1:c.3277G= XP_011530776.1:p.Ala1093=
XM_017003117.1:c.3199G= XP_016858606.1:p.Ala1067=
XR_002958896.1:n.3319G=
NM_133259.4:c.3277G= MANE Select NP_573566.2:p.Ala1093=