Canonical Allele Identifier: CA2493981257
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43905750C= , CM000664.2:g.43905750C= GRCh38
NC_000002.11:g.44132889C= , CM000664.1:g.44132889C= GRCh37
NC_000002.10:g.43986393C= NCBI36
NG_008247.1:g.95256G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000472420.6:n.385G=
ENST00000681993.1:n.858G=
ENST00000682295.1:c.461G= ENSP00000507499.1:n.461G=
ENST00000682303.1:c.*3092G= ENSP00000508325.1:n.*3092G=
ENST00000682308.1:c.3306G= ENSP00000507056.1:p.Leu1102=
ENST00000682480.1:c.3324G= ENSP00000508344.1:p.Leu1108=
ENST00000682546.1:c.3303G= ENSP00000508188.1:p.Leu1101=
ENST00000682585.1:c.3306G= ENSP00000506885.1:p.Leu1102=
ENST00000682595.1:n.3890G=
ENST00000682607.1:c.1724G=
ENST00000682612.1:c.158G=
ENST00000682779.1:c.3297G= ENSP00000507947.1:p.Leu1099=
ENST00000682845.1:n.2408G=
ENST00000682885.1:c.3261G= ENSP00000508036.1:p.Leu1087=
ENST00000682933.1:n.3380G=
ENST00000683002.1:c.158G=
ENST00000683072.1:n.3890G=
ENST00000683080.1:n.925G=
ENST00000683125.1:c.3414G= ENSP00000507939.1:p.Leu1138=
ENST00000683213.1:c.3309G= ENSP00000507751.1:p.Leu1103=
ENST00000683220.1:c.3336G= ENSP00000507151.1:p.Leu1112=
ENST00000683329.1:n.4109G=
ENST00000683346.1:c.*3181G= ENSP00000507458.1:n.*3181G=
ENST00000683409.1:n.1913G=
ENST00000683459.1:n.3893G=
ENST00000683528.1:c.158G=
ENST00000683590.1:c.3054G= ENSP00000506820.1:p.Leu1018=
ENST00000683623.1:c.3213G= ENSP00000507702.1:p.Leu1071=
ENST00000683645.1:n.3857G=
ENST00000683796.1:c.*3178G= ENSP00000508221.1:n.*3178G=
ENST00000683802.1:n.6231G=
ENST00000683833.1:c.3297G= ENSP00000506852.1:p.Leu1099=
ENST00000683994.1:c.3306G= ENSP00000507181.1:p.Leu1102=
ENST00000684290.1:c.*842G= ENSP00000507243.1:n.*842G=
ENST00000684306.1:c.*3219G= ENSP00000508384.1:n.*3219G=
ENST00000684341.1:n.3326G=
ENST00000684383.1:c.*2944G= ENSP00000506863.1:n.*2944G=
ENST00000684418.1:n.4487G=
ENST00000684454.1:n.2656G=
ENST00000684619.1:c.*3178G= ENSP00000508088.1:n.*3178G=
ENST00000684743.1:n.4337G=
ENST00000260665.12:c.3306G= MANE Select ENSP00000260665.7:p.Leu1102=
ENST00000260665.11:c.3306G= ENSP00000260665.7:p.Leu1102=
NM_133259.3:c.3306G= NP_573566.2:p.Leu1102=
XM_006711915.2:c.3228G= XP_006711978.1:p.Leu1076=
XM_011532473.1:c.3306G= XP_011530775.1:p.Leu1102=
XM_011532474.1:c.3306G= XP_011530776.1:p.Leu1102=
XM_017003117.1:c.3228G= XP_016858606.1:p.Leu1076=
XR_002958896.1:n.3348G=
NM_133259.4:c.3306G= MANE Select NP_573566.2:p.Leu1102=