Canonical Allele Identifier: CA2493988254
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43918396T= , CM000664.2:g.43918396T= GRCh38
NC_000002.11:g.44145535T= , CM000664.1:g.44145535T= GRCh37
NC_000002.10:g.43999039T= NCBI36
NG_008247.1:g.82610A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681993.1:n.451A=
ENST00000682295.1:c.163A= ENSP00000507499.1:p.Ile55=
ENST00000682303.1:c.*2685A= ENSP00000508325.1:n.*2685A=
ENST00000682308.1:c.2899A= ENSP00000507056.1:p.Ile967=
ENST00000682480.1:c.2899A= ENSP00000508344.1:p.Ile967=
ENST00000682546.1:c.2896A= ENSP00000508188.1:p.Ile966=
ENST00000682585.1:c.2899A= ENSP00000506885.1:p.Ile967=
ENST00000682595.1:n.3483A=
ENST00000682607.1:c.1317A=
ENST00000682779.1:c.2890A= ENSP00000507947.1:p.Ile964=
ENST00000682845.1:n.2001A=
ENST00000682885.1:c.2854A= ENSP00000508036.1:p.Ile952=
ENST00000682933.1:n.2973A=
ENST00000683072.1:n.3483A=
ENST00000683080.1:n.518A=
ENST00000683125.1:c.3007A= ENSP00000507939.1:p.Ile1003=
ENST00000683213.1:c.2902A= ENSP00000507751.1:p.Ile968=
ENST00000683220.1:c.2929A= ENSP00000507151.1:p.Ile977=
ENST00000683236.1:c.229A= ENSP00000506891.1:n.229A=
ENST00000683329.1:n.3702A=
ENST00000683346.1:c.*2774A= ENSP00000507458.1:n.*2774A=
ENST00000683409.1:n.1506A=
ENST00000683459.1:n.3486A=
ENST00000683590.1:c.2897-5838A= ENSP00000506820.1:n.2897-5838A=
ENST00000683623.1:c.2806A= ENSP00000507702.1:p.Ile936=
ENST00000683645.1:n.3450A=
ENST00000683796.1:c.*2771A= ENSP00000508221.1:n.*2771A=
ENST00000683802.1:n.5824A=
ENST00000683833.1:c.2890A= ENSP00000506852.1:p.Ile964=
ENST00000683994.1:c.2899A= ENSP00000507181.1:p.Ile967=
ENST00000684290.1:c.*435A= ENSP00000507243.1:n.*435A=
ENST00000684306.1:c.*2812A= ENSP00000508384.1:n.*2812A=
ENST00000684341.1:n.2919A=
ENST00000684383.1:c.*2537A= ENSP00000506863.1:n.*2537A=
ENST00000684619.1:c.*2771A= ENSP00000508088.1:n.*2771A=
ENST00000684705.1:n.20A=
ENST00000684743.1:n.3930A=
ENST00000260665.12:c.2899A= MANE Select ENSP00000260665.7:p.Ile967=
ENST00000260665.11:c.2899A= ENSP00000260665.7:p.Ile967=
NM_133259.3:c.2899A= NP_573566.2:p.Ile967=
XM_006711915.2:c.2821A= XP_006711978.1:p.Ile941=
XM_006711916.2:c.2899A= XP_006711979.1:p.Ile967=
XM_011532473.1:c.2899A= XP_011530775.1:p.Ile967=
XM_011532474.1:c.2899A= XP_011530776.1:p.Ile967=
XM_006711916.3:c.2899A= XP_006711979.1:p.Ile967=
XM_017003117.1:c.2821A= XP_016858606.1:p.Ile941=
XR_002958896.1:n.2941A=
NM_133259.4:c.2899A= MANE Select NP_573566.2:p.Ile967=