Canonical Allele Identifier: CA2493981233
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43905707G= , CM000664.2:g.43905707G= GRCh38
NC_000002.11:g.44132846G= , CM000664.1:g.44132846G= GRCh37
NC_000002.10:g.43986350G= NCBI36
NG_008247.1:g.95299C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000472420.6:n.428C=
ENST00000681993.1:n.901C=
ENST00000682295.1:c.504C= ENSP00000507499.1:n.504C=
ENST00000682303.1:c.*3135C= ENSP00000508325.1:n.*3135C=
ENST00000682308.1:c.3349C= ENSP00000507056.1:p.Arg1117=
ENST00000682480.1:c.3367C= ENSP00000508344.1:p.Arg1123=
ENST00000682546.1:c.3346C= ENSP00000508188.1:p.Arg1116=
ENST00000682585.1:c.3349C= ENSP00000506885.1:p.Arg1117=
ENST00000682595.1:n.3933C=
ENST00000682607.1:c.1767C=
ENST00000682612.1:c.201C=
ENST00000682779.1:c.3340C= ENSP00000507947.1:p.Arg1114=
ENST00000682845.1:n.2451C=
ENST00000682885.1:c.3304C= ENSP00000508036.1:p.Arg1102=
ENST00000682933.1:n.3423C=
ENST00000683002.1:c.201C=
ENST00000683072.1:n.3933C=
ENST00000683080.1:n.968C=
ENST00000683125.1:c.3457C= ENSP00000507939.1:p.Arg1153=
ENST00000683213.1:c.3352C= ENSP00000507751.1:p.Arg1118=
ENST00000683220.1:c.3379C= ENSP00000507151.1:p.Arg1127=
ENST00000683329.1:n.4152C=
ENST00000683346.1:c.*3224C= ENSP00000507458.1:n.*3224C=
ENST00000683409.1:n.1956C=
ENST00000683459.1:n.3936C=
ENST00000683528.1:c.201C=
ENST00000683590.1:c.3097C= ENSP00000506820.1:p.Arg1033=
ENST00000683623.1:c.3256C= ENSP00000507702.1:p.Arg1086=
ENST00000683645.1:n.3900C=
ENST00000683796.1:c.*3221C= ENSP00000508221.1:n.*3221C=
ENST00000683802.1:n.6274C=
ENST00000683833.1:c.3340C= ENSP00000506852.1:p.Arg1114=
ENST00000683994.1:c.3349C= ENSP00000507181.1:p.Arg1117=
ENST00000684290.1:c.*885C= ENSP00000507243.1:n.*885C=
ENST00000684306.1:c.*3262C= ENSP00000508384.1:n.*3262C=
ENST00000684341.1:n.3369C=
ENST00000684383.1:c.*2987C= ENSP00000506863.1:n.*2987C=
ENST00000684418.1:n.4530C=
ENST00000684454.1:n.2699C=
ENST00000684619.1:c.*3221C= ENSP00000508088.1:n.*3221C=
ENST00000684743.1:n.4380C=
ENST00000260665.12:c.3349C= MANE Select ENSP00000260665.7:p.Arg1117=
ENST00000260665.11:c.3349C= ENSP00000260665.7:p.Arg1117=
NM_133259.3:c.3349C= NP_573566.2:p.Arg1117=
XM_006711915.2:c.3271C= XP_006711978.1:p.Arg1091=
XM_011532473.1:c.3349C= XP_011530775.1:p.Arg1117=
XM_011532474.1:c.3349C= XP_011530776.1:p.Arg1117=
XM_017003117.1:c.3271C= XP_016858606.1:p.Arg1091=
XR_002958896.1:n.3391C=
NM_133259.4:c.3349C= MANE Select NP_573566.2:p.Arg1117=