Canonical Allele Identifier: CA2493988218
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43918324T= , CM000664.2:g.43918324T= GRCh38
NC_000002.11:g.44145463T= , CM000664.1:g.44145463T= GRCh37
NC_000002.10:g.43998967T= NCBI36
NG_008247.1:g.82682A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681993.1:n.523A=
ENST00000682295.1:c.235A= ENSP00000507499.1:p.Lys79=
ENST00000682303.1:c.*2757A= ENSP00000508325.1:n.*2757A=
ENST00000682308.1:c.2971A= ENSP00000507056.1:p.Lys991=
ENST00000682480.1:c.2971A= ENSP00000508344.1:p.Lys991=
ENST00000682546.1:c.2968A= ENSP00000508188.1:p.Lys990=
ENST00000682585.1:c.2971A= ENSP00000506885.1:p.Lys991=
ENST00000682595.1:n.3555A=
ENST00000682607.1:c.1389A=
ENST00000682779.1:c.2962A= ENSP00000507947.1:p.Lys988=
ENST00000682845.1:n.2073A=
ENST00000682885.1:c.2926A= ENSP00000508036.1:p.Lys976=
ENST00000682933.1:n.3045A=
ENST00000683072.1:n.3555A=
ENST00000683080.1:n.590A=
ENST00000683125.1:c.3079A= ENSP00000507939.1:p.Lys1027=
ENST00000683213.1:c.2974A= ENSP00000507751.1:p.Lys992=
ENST00000683220.1:c.3001A= ENSP00000507151.1:p.Lys1001=
ENST00000683236.1:c.301A= ENSP00000506891.1:n.301A=
ENST00000683329.1:n.3774A=
ENST00000683346.1:c.*2846A= ENSP00000507458.1:n.*2846A=
ENST00000683409.1:n.1578A=
ENST00000683459.1:n.3558A=
ENST00000683590.1:c.2897-5766A= ENSP00000506820.1:n.2897-5766A=
ENST00000683623.1:c.2878A= ENSP00000507702.1:p.Lys960=
ENST00000683645.1:n.3522A=
ENST00000683796.1:c.*2843A= ENSP00000508221.1:n.*2843A=
ENST00000683802.1:n.5896A=
ENST00000683833.1:c.2962A= ENSP00000506852.1:p.Lys988=
ENST00000683994.1:c.2971A= ENSP00000507181.1:p.Lys991=
ENST00000684290.1:c.*507A= ENSP00000507243.1:n.*507A=
ENST00000684306.1:c.*2884A= ENSP00000508384.1:n.*2884A=
ENST00000684341.1:n.2991A=
ENST00000684383.1:c.*2609A= ENSP00000506863.1:n.*2609A=
ENST00000684619.1:c.*2843A= ENSP00000508088.1:n.*2843A=
ENST00000684705.1:n.92A=
ENST00000684743.1:n.4002A=
ENST00000260665.12:c.2971A= MANE Select ENSP00000260665.7:p.Lys991=
ENST00000260665.11:c.2971A= ENSP00000260665.7:p.Lys991=
NM_133259.3:c.2971A= NP_573566.2:p.Lys991=
XM_006711915.2:c.2893A= XP_006711978.1:p.Lys965=
XM_006711916.2:c.2971A= XP_006711979.1:p.Lys991=
XM_011532473.1:c.2971A= XP_011530775.1:p.Lys991=
XM_011532474.1:c.2971A= XP_011530776.1:p.Lys991=
XM_006711916.3:c.2971A= XP_006711979.1:p.Lys991=
XM_017003117.1:c.2893A= XP_016858606.1:p.Lys965=
XR_002958896.1:n.3013A=
NM_133259.4:c.2971A= MANE Select NP_573566.2:p.Lys991=