Canonical Allele Identifier: CA2493977956
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43899322G= , CM000664.2:g.43899322G= GRCh38
NC_000002.11:g.44126461G= , CM000664.1:g.44126461G= GRCh37
NC_000002.10:g.43979965G= NCBI36
NG_008247.1:g.101684C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000419884.6:c.153C=
ENST00000472420.6:n.801C=
ENST00000483489.2:n.153C=
ENST00000681993.1:n.1274C=
ENST00000682303.1:c.*3508C= ENSP00000508325.1:n.*3508C=
ENST00000682308.1:c.3722C= ENSP00000507056.1:p.Ala1241=
ENST00000682434.1:n.1273C=
ENST00000682480.1:c.3740C= ENSP00000508344.1:p.Ala1247=
ENST00000682546.1:c.3719C= ENSP00000508188.1:p.Ala1240=
ENST00000682585.1:c.3722C= ENSP00000506885.1:p.Ala1241=
ENST00000682595.1:n.4306C=
ENST00000682607.1:c.2140C=
ENST00000682612.1:c.574C=
ENST00000682779.1:c.3713C= ENSP00000507947.1:p.Ala1238=
ENST00000682845.1:n.2824C=
ENST00000682885.1:c.3677C= ENSP00000508036.1:p.Ala1226=
ENST00000682933.1:n.3796C=
ENST00000683002.1:c.574C=
ENST00000683072.1:n.4306C=
ENST00000683080.1:n.1341C=
ENST00000683125.1:c.3830C= ENSP00000507939.1:p.Ala1277=
ENST00000683213.1:c.3725C= ENSP00000507751.1:p.Ala1242=
ENST00000683220.1:c.3752C= ENSP00000507151.1:p.Ala1251=
ENST00000683329.1:n.4525C=
ENST00000683346.1:c.*3597C= ENSP00000507458.1:n.*3597C=
ENST00000683409.1:n.2329C=
ENST00000683459.1:n.4309C=
ENST00000683528.1:c.650C=
ENST00000683590.1:c.3470C= ENSP00000506820.1:p.Ala1157=
ENST00000683623.1:c.3629C= ENSP00000507702.1:p.Ala1210=
ENST00000683645.1:n.4273C=
ENST00000683796.1:c.*3594C= ENSP00000508221.1:n.*3594C=
ENST00000683802.1:n.6647C=
ENST00000683833.1:c.3713C= ENSP00000506852.1:p.Ala1238=
ENST00000683994.1:c.3722C= ENSP00000507181.1:p.Ala1241=
ENST00000684290.1:c.*1258C= ENSP00000507243.1:n.*1258C=
ENST00000684306.1:c.*3635C= ENSP00000508384.1:n.*3635C=
ENST00000684341.1:n.3742C=
ENST00000684383.1:c.*3360C= ENSP00000506863.1:n.*3360C=
ENST00000684418.1:n.4903C=
ENST00000684433.1:n.106C=
ENST00000684454.1:n.3072C=
ENST00000684619.1:c.*3594C= ENSP00000508088.1:n.*3594C=
ENST00000684743.1:n.6467C=
ENST00000260665.12:c.3722C= MANE Select ENSP00000260665.7:p.Ala1241=
ENST00000260665.11:c.3722C= ENSP00000260665.7:p.Ala1241=
ENST00000463456.5:n.2765C=
ENST00000472420.5:n.119C=
ENST00000483489.1:n.196C=
NM_133259.3:c.3722C= NP_573566.2:p.Ala1241=
XM_006711915.2:c.3644C= XP_006711978.1:p.Ala1215=
XM_011532473.1:c.3722C= XP_011530775.1:p.Ala1241=
XM_011532474.1:c.3722C= XP_011530776.1:p.Ala1241=
XM_017003117.1:c.3644C= XP_016858606.1:p.Ala1215=
XR_002958896.1:n.3764C=
NM_133259.4:c.3722C= MANE Select NP_573566.2:p.Ala1241=