Canonical Allele Identifier: CA2493988246
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43918384A= , CM000664.2:g.43918384A= GRCh38
NC_000002.11:g.44145523A= , CM000664.1:g.44145523A= GRCh37
NC_000002.10:g.43999027A= NCBI36
NG_008247.1:g.82622T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681993.1:n.463T=
ENST00000682295.1:c.175T= ENSP00000507499.1:p.Trp59=
ENST00000682303.1:c.*2697T= ENSP00000508325.1:n.*2697T=
ENST00000682308.1:c.2911T= ENSP00000507056.1:p.Trp971=
ENST00000682480.1:c.2911T= ENSP00000508344.1:p.Trp971=
ENST00000682546.1:c.2908T= ENSP00000508188.1:p.Trp970=
ENST00000682585.1:c.2911T= ENSP00000506885.1:p.Trp971=
ENST00000682595.1:n.3495T=
ENST00000682607.1:c.1329T=
ENST00000682779.1:c.2902T= ENSP00000507947.1:p.Trp968=
ENST00000682845.1:n.2013T=
ENST00000682885.1:c.2866T= ENSP00000508036.1:p.Trp956=
ENST00000682933.1:n.2985T=
ENST00000683072.1:n.3495T=
ENST00000683080.1:n.530T=
ENST00000683125.1:c.3019T= ENSP00000507939.1:p.Trp1007=
ENST00000683213.1:c.2914T= ENSP00000507751.1:p.Trp972=
ENST00000683220.1:c.2941T= ENSP00000507151.1:p.Trp981=
ENST00000683236.1:c.241T= ENSP00000506891.1:n.241T=
ENST00000683329.1:n.3714T=
ENST00000683346.1:c.*2786T= ENSP00000507458.1:n.*2786T=
ENST00000683409.1:n.1518T=
ENST00000683459.1:n.3498T=
ENST00000683590.1:c.2897-5826T= ENSP00000506820.1:n.2897-5826T=
ENST00000683623.1:c.2818T= ENSP00000507702.1:p.Trp940=
ENST00000683645.1:n.3462T=
ENST00000683796.1:c.*2783T= ENSP00000508221.1:n.*2783T=
ENST00000683802.1:n.5836T=
ENST00000683833.1:c.2902T= ENSP00000506852.1:p.Trp968=
ENST00000683994.1:c.2911T= ENSP00000507181.1:p.Trp971=
ENST00000684290.1:c.*447T= ENSP00000507243.1:n.*447T=
ENST00000684306.1:c.*2824T= ENSP00000508384.1:n.*2824T=
ENST00000684341.1:n.2931T=
ENST00000684383.1:c.*2549T= ENSP00000506863.1:n.*2549T=
ENST00000684619.1:c.*2783T= ENSP00000508088.1:n.*2783T=
ENST00000684705.1:n.32T=
ENST00000684743.1:n.3942T=
ENST00000260665.12:c.2911T= MANE Select ENSP00000260665.7:p.Trp971=
ENST00000260665.11:c.2911T= ENSP00000260665.7:p.Trp971=
NM_133259.3:c.2911T= NP_573566.2:p.Trp971=
XM_006711915.2:c.2833T= XP_006711978.1:p.Trp945=
XM_006711916.2:c.2911T= XP_006711979.1:p.Trp971=
XM_011532473.1:c.2911T= XP_011530775.1:p.Trp971=
XM_011532474.1:c.2911T= XP_011530776.1:p.Trp971=
XM_006711916.3:c.2911T= XP_006711979.1:p.Trp971=
XM_017003117.1:c.2833T= XP_016858606.1:p.Trp945=
XR_002958896.1:n.2953T=
NM_133259.4:c.2911T= MANE Select NP_573566.2:p.Trp971=