Canonical Allele Identifier: CA2493981268
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43905767T= , CM000664.2:g.43905767T= GRCh38
NC_000002.11:g.44132906T= , CM000664.1:g.44132906T= GRCh37
NC_000002.10:g.43986410T= NCBI36
NG_008247.1:g.95239A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000472420.6:n.368A=
ENST00000681993.1:n.841A=
ENST00000682295.1:c.444A= ENSP00000507499.1:n.444A=
ENST00000682303.1:c.*3075A= ENSP00000508325.1:n.*3075A=
ENST00000682308.1:c.3289A= ENSP00000507056.1:p.Ile1097=
ENST00000682480.1:c.3307A= ENSP00000508344.1:p.Ile1103=
ENST00000682546.1:c.3286A= ENSP00000508188.1:p.Ile1096=
ENST00000682585.1:c.3289A= ENSP00000506885.1:p.Ile1097=
ENST00000682595.1:n.3873A=
ENST00000682607.1:c.1707A=
ENST00000682612.1:c.141A=
ENST00000682779.1:c.3280A= ENSP00000507947.1:p.Ile1094=
ENST00000682845.1:n.2391A=
ENST00000682885.1:c.3244A= ENSP00000508036.1:p.Ile1082=
ENST00000682933.1:n.3363A=
ENST00000683002.1:c.141A=
ENST00000683072.1:n.3873A=
ENST00000683080.1:n.908A=
ENST00000683125.1:c.3397A= ENSP00000507939.1:p.Ile1133=
ENST00000683213.1:c.3292A= ENSP00000507751.1:p.Ile1098=
ENST00000683220.1:c.3319A= ENSP00000507151.1:p.Ile1107=
ENST00000683329.1:n.4092A=
ENST00000683346.1:c.*3164A= ENSP00000507458.1:n.*3164A=
ENST00000683409.1:n.1896A=
ENST00000683459.1:n.3876A=
ENST00000683528.1:c.141A=
ENST00000683590.1:c.3037A= ENSP00000506820.1:p.Ile1013=
ENST00000683623.1:c.3196A= ENSP00000507702.1:p.Ile1066=
ENST00000683645.1:n.3840A=
ENST00000683796.1:c.*3161A= ENSP00000508221.1:n.*3161A=
ENST00000683802.1:n.6214A=
ENST00000683833.1:c.3280A= ENSP00000506852.1:p.Ile1094=
ENST00000683994.1:c.3289A= ENSP00000507181.1:p.Ile1097=
ENST00000684290.1:c.*825A= ENSP00000507243.1:n.*825A=
ENST00000684306.1:c.*3202A= ENSP00000508384.1:n.*3202A=
ENST00000684341.1:n.3309A=
ENST00000684383.1:c.*2927A= ENSP00000506863.1:n.*2927A=
ENST00000684418.1:n.4470A=
ENST00000684454.1:n.2639A=
ENST00000684619.1:c.*3161A= ENSP00000508088.1:n.*3161A=
ENST00000684743.1:n.4320A=
ENST00000260665.12:c.3289A= MANE Select ENSP00000260665.7:p.Ile1097=
ENST00000260665.11:c.3289A= ENSP00000260665.7:p.Ile1097=
NM_133259.3:c.3289A= NP_573566.2:p.Ile1097=
XM_006711915.2:c.3211A= XP_006711978.1:p.Ile1071=
XM_011532473.1:c.3289A= XP_011530775.1:p.Ile1097=
XM_011532474.1:c.3289A= XP_011530776.1:p.Ile1097=
XM_017003117.1:c.3211A= XP_016858606.1:p.Ile1071=
XR_002958896.1:n.3331A=
NM_133259.4:c.3289A= MANE Select NP_573566.2:p.Ile1097=