Canonical Allele Identifier: CA2493981245
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43905725T= , CM000664.2:g.43905725T= GRCh38
NC_000002.11:g.44132864T= , CM000664.1:g.44132864T= GRCh37
NC_000002.10:g.43986368T= NCBI36
NG_008247.1:g.95281A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000472420.6:n.410A=
ENST00000681993.1:n.883A=
ENST00000682295.1:c.486A= ENSP00000507499.1:n.486A=
ENST00000682303.1:c.*3117A= ENSP00000508325.1:n.*3117A=
ENST00000682308.1:c.3331A= ENSP00000507056.1:p.Ile1111=
ENST00000682480.1:c.3349A= ENSP00000508344.1:p.Ile1117=
ENST00000682546.1:c.3328A= ENSP00000508188.1:p.Ile1110=
ENST00000682585.1:c.3331A= ENSP00000506885.1:p.Ile1111=
ENST00000682595.1:n.3915A=
ENST00000682607.1:c.1749A=
ENST00000682612.1:c.183A=
ENST00000682779.1:c.3322A= ENSP00000507947.1:p.Ile1108=
ENST00000682845.1:n.2433A=
ENST00000682885.1:c.3286A= ENSP00000508036.1:p.Ile1096=
ENST00000682933.1:n.3405A=
ENST00000683002.1:c.183A=
ENST00000683072.1:n.3915A=
ENST00000683080.1:n.950A=
ENST00000683125.1:c.3439A= ENSP00000507939.1:p.Ile1147=
ENST00000683213.1:c.3334A= ENSP00000507751.1:p.Ile1112=
ENST00000683220.1:c.3361A= ENSP00000507151.1:p.Ile1121=
ENST00000683329.1:n.4134A=
ENST00000683346.1:c.*3206A= ENSP00000507458.1:n.*3206A=
ENST00000683409.1:n.1938A=
ENST00000683459.1:n.3918A=
ENST00000683528.1:c.183A=
ENST00000683590.1:c.3079A= ENSP00000506820.1:p.Ile1027=
ENST00000683623.1:c.3238A= ENSP00000507702.1:p.Ile1080=
ENST00000683645.1:n.3882A=
ENST00000683796.1:c.*3203A= ENSP00000508221.1:n.*3203A=
ENST00000683802.1:n.6256A=
ENST00000683833.1:c.3322A= ENSP00000506852.1:p.Ile1108=
ENST00000683994.1:c.3331A= ENSP00000507181.1:p.Ile1111=
ENST00000684290.1:c.*867A= ENSP00000507243.1:n.*867A=
ENST00000684306.1:c.*3244A= ENSP00000508384.1:n.*3244A=
ENST00000684341.1:n.3351A=
ENST00000684383.1:c.*2969A= ENSP00000506863.1:n.*2969A=
ENST00000684418.1:n.4512A=
ENST00000684454.1:n.2681A=
ENST00000684619.1:c.*3203A= ENSP00000508088.1:n.*3203A=
ENST00000684743.1:n.4362A=
ENST00000260665.12:c.3331A= MANE Select ENSP00000260665.7:p.Ile1111=
ENST00000260665.11:c.3331A= ENSP00000260665.7:p.Ile1111=
NM_133259.3:c.3331A= NP_573566.2:p.Ile1111=
XM_006711915.2:c.3253A= XP_006711978.1:p.Ile1085=
XM_011532473.1:c.3331A= XP_011530775.1:p.Ile1111=
XM_011532474.1:c.3331A= XP_011530776.1:p.Ile1111=
XM_017003117.1:c.3253A= XP_016858606.1:p.Ile1085=
XR_002958896.1:n.3373A=
NM_133259.4:c.3331A= MANE Select NP_573566.2:p.Ile1111=