Canonical Allele Identifier: CA2494001918
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43943781T= , CM000664.2:g.43943781T= GRCh38
NC_000002.11:g.44170920T= , CM000664.1:g.44170920T= GRCh37
NC_000002.10:g.44024424T= NCBI36
NG_008247.1:g.57225A=

Transcript Alleles

HGVS Amino-acid change
ENST00000409659.6:c.2410A= ENSP00000386562.2:p.Thr804=
ENST00000447246.2:c.2410A= ENSP00000403637.2:p.Thr804=
ENST00000681961.1:n.2430A=
ENST00000682104.1:c.2284A= ENSP00000507716.1:p.Thr762=
ENST00000682303.1:c.*2196A= ENSP00000508325.1:n.*2196A=
ENST00000682308.1:c.2410A= ENSP00000507056.1:p.Thr804=
ENST00000682480.1:c.2410A= ENSP00000508344.1:p.Thr804=
ENST00000682546.1:c.2407A= ENSP00000508188.1:p.Thr803=
ENST00000682585.1:c.2410A= ENSP00000506885.1:p.Thr804=
ENST00000682595.1:n.2992A=
ENST00000682607.1:c.828A=
ENST00000682779.1:c.2401A= ENSP00000507947.1:p.Thr801=
ENST00000682845.1:n.1512A=
ENST00000682885.1:c.2365A= ENSP00000508036.1:p.Thr789=
ENST00000682933.1:n.2484A=
ENST00000683072.1:n.2992A=
ENST00000683125.1:c.2410A= ENSP00000507939.1:p.Thr804=
ENST00000683213.1:c.2413A= ENSP00000507751.1:p.Thr805=
ENST00000683220.1:c.2440A= ENSP00000507151.1:p.Thr814=
ENST00000683329.1:n.3213A=
ENST00000683346.1:c.*2285A= ENSP00000507458.1:n.*2285A=
ENST00000683459.1:n.2997A=
ENST00000683590.1:c.2410A= ENSP00000506820.1:p.Thr804=
ENST00000683623.1:c.2317A= ENSP00000507702.1:p.Thr773=
ENST00000683645.1:n.2961A=
ENST00000683694.1:n.1161A=
ENST00000683796.1:c.*2282A= ENSP00000508221.1:n.*2282A=
ENST00000683802.1:n.5335A=
ENST00000683833.1:c.2401A= ENSP00000506852.1:p.Thr801=
ENST00000683989.1:c.2410A= ENSP00000507510.1:p.Thr804=
ENST00000683994.1:c.2410A= ENSP00000507181.1:p.Thr804=
ENST00000684290.1:c.*104A= ENSP00000507243.1:n.*104A=
ENST00000684306.1:c.*2323A= ENSP00000508384.1:n.*2323A=
ENST00000684341.1:n.2430A=
ENST00000684383.1:c.*2048A= ENSP00000506863.1:n.*2048A=
ENST00000684397.1:c.114A=
ENST00000684619.1:c.*2282A= ENSP00000508088.1:n.*2282A=
ENST00000684743.1:n.3441A=
ENST00000260665.12:c.2410A= MANE Select ENSP00000260665.7:p.Thr804=
ENST00000260665.11:c.2410A= ENSP00000260665.7:p.Thr804=
NM_133259.3:c.2410A= NP_573566.2:p.Thr804=
XM_006711915.2:c.2332A= XP_006711978.1:p.Thr778=
XM_006711916.2:c.2410A= XP_006711979.1:p.Thr804=
XM_011532473.1:c.2410A= XP_011530775.1:p.Thr804=
XM_011532474.1:c.2410A= XP_011530776.1:p.Thr804=
XM_006711916.3:c.2410A= XP_006711979.1:p.Thr804=
XM_017003117.1:c.2332A= XP_016858606.1:p.Thr778=
XR_002958896.1:n.2452A=
NM_133259.4:c.2410A= MANE Select NP_573566.2:p.Thr804=