Canonical Allele Identifier: CA2493988091
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43918044G= , CM000664.2:g.43918044G= GRCh38
NC_000002.11:g.44145183G= , CM000664.1:g.44145183G= GRCh37
NC_000002.10:g.43998687G= NCBI36
NG_008247.1:g.82962C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681993.1:n.681C=
ENST00000682295.1:c.303+212C= ENSP00000507499.1:n.303+212C=
ENST00000682303.1:c.*2915C= ENSP00000508325.1:n.*2915C=
ENST00000682308.1:c.3129C= ENSP00000507056.1:p.Cys1043=
ENST00000682480.1:c.3147C= ENSP00000508344.1:p.Cys1049=
ENST00000682546.1:c.3126C= ENSP00000508188.1:p.Cys1042=
ENST00000682585.1:c.3129C= ENSP00000506885.1:p.Cys1043=
ENST00000682595.1:n.3713C=
ENST00000682607.1:c.1547C=
ENST00000682779.1:c.3120C= ENSP00000507947.1:p.Cys1040=
ENST00000682845.1:n.2231C=
ENST00000682885.1:c.3084C= ENSP00000508036.1:p.Cys1028=
ENST00000682933.1:n.3203C=
ENST00000683072.1:n.3713C=
ENST00000683080.1:n.748C=
ENST00000683125.1:c.3237C= ENSP00000507939.1:p.Cys1079=
ENST00000683213.1:c.3132C= ENSP00000507751.1:p.Cys1044=
ENST00000683220.1:c.3159C= ENSP00000507151.1:p.Cys1053=
ENST00000683329.1:n.3932C=
ENST00000683346.1:c.*3004C= ENSP00000507458.1:n.*3004C=
ENST00000683409.1:n.1736C=
ENST00000683459.1:n.3716C=
ENST00000683590.1:c.2897-5486C= ENSP00000506820.1:n.2897-5486C=
ENST00000683623.1:c.3036C= ENSP00000507702.1:p.Cys1012=
ENST00000683645.1:n.3680C=
ENST00000683796.1:c.*3001C= ENSP00000508221.1:n.*3001C=
ENST00000683802.1:n.6054C=
ENST00000683833.1:c.3120C= ENSP00000506852.1:p.Cys1040=
ENST00000683994.1:c.3129C= ENSP00000507181.1:p.Cys1043=
ENST00000684290.1:c.*665C= ENSP00000507243.1:n.*665C=
ENST00000684306.1:c.*3042C= ENSP00000508384.1:n.*3042C=
ENST00000684341.1:n.3149C=
ENST00000684383.1:c.*2767C= ENSP00000506863.1:n.*2767C=
ENST00000684619.1:c.*3001C= ENSP00000508088.1:n.*3001C=
ENST00000684705.1:n.250C=
ENST00000684743.1:n.4160C=
ENST00000260665.12:c.3129C= MANE Select ENSP00000260665.7:p.Cys1043=
ENST00000260665.11:c.3129C= ENSP00000260665.7:p.Cys1043=
NM_133259.3:c.3129C= NP_573566.2:p.Cys1043=
XM_006711915.2:c.3051C= XP_006711978.1:p.Cys1017=
XM_006711916.2:c.3129C= XP_006711979.1:p.Cys1043=
XM_011532473.1:c.3129C= XP_011530775.1:p.Cys1043=
XM_011532474.1:c.3129C= XP_011530776.1:p.Cys1043=
XM_006711916.3:c.3129C= XP_006711979.1:p.Cys1043=
XM_017003117.1:c.3051C= XP_016858606.1:p.Cys1017=
XR_002958896.1:n.3171C=
NM_133259.4:c.3129C= MANE Select NP_573566.2:p.Cys1043=