Canonical Allele Identifier: CA2494001899
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43943730A= , CM000664.2:g.43943730A= GRCh38
NC_000002.11:g.44170869A= , CM000664.1:g.44170869A= GRCh37
NC_000002.10:g.44024373A= NCBI36
NG_008247.1:g.57276T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409659.6:c.2461T= ENSP00000386562.2:p.Ser821=
ENST00000447246.2:c.2461T= ENSP00000403637.2:p.Ser821=
ENST00000681961.1:n.2481T=
ENST00000682104.1:c.2335T= ENSP00000507716.1:p.Ser779=
ENST00000682303.1:c.*2247T= ENSP00000508325.1:n.*2247T=
ENST00000682308.1:c.2461T= ENSP00000507056.1:p.Ser821=
ENST00000682480.1:c.2461T= ENSP00000508344.1:p.Ser821=
ENST00000682546.1:c.2458T= ENSP00000508188.1:p.Ser820=
ENST00000682585.1:c.2461T= ENSP00000506885.1:p.Ser821=
ENST00000682595.1:n.3043T=
ENST00000682607.1:c.879T=
ENST00000682779.1:c.2452T= ENSP00000507947.1:p.Ser818=
ENST00000682845.1:n.1563T=
ENST00000682885.1:c.2416T= ENSP00000508036.1:p.Ser806=
ENST00000682933.1:n.2535T=
ENST00000683072.1:n.3043T=
ENST00000683125.1:c.2461T= ENSP00000507939.1:p.Ser821=
ENST00000683213.1:c.2464T= ENSP00000507751.1:p.Ser822=
ENST00000683220.1:c.2491T= ENSP00000507151.1:p.Ser831=
ENST00000683329.1:n.3264T=
ENST00000683346.1:c.*2336T= ENSP00000507458.1:n.*2336T=
ENST00000683459.1:n.3048T=
ENST00000683590.1:c.2461T= ENSP00000506820.1:p.Ser821=
ENST00000683623.1:c.2368T= ENSP00000507702.1:p.Ser790=
ENST00000683645.1:n.3012T=
ENST00000683694.1:n.1212T=
ENST00000683796.1:c.*2333T= ENSP00000508221.1:n.*2333T=
ENST00000683802.1:n.5386T=
ENST00000683833.1:c.2452T= ENSP00000506852.1:p.Ser818=
ENST00000683989.1:c.2461T= ENSP00000507510.1:p.Ser821=
ENST00000683994.1:c.2461T= ENSP00000507181.1:p.Ser821=
ENST00000684290.1:c.*155T= ENSP00000507243.1:n.*155T=
ENST00000684306.1:c.*2374T= ENSP00000508384.1:n.*2374T=
ENST00000684341.1:n.2481T=
ENST00000684383.1:c.*2099T= ENSP00000506863.1:n.*2099T=
ENST00000684397.1:c.165T=
ENST00000684619.1:c.*2333T= ENSP00000508088.1:n.*2333T=
ENST00000684743.1:n.3492T=
ENST00000260665.12:c.2461T= MANE Select ENSP00000260665.7:p.Ser821=
ENST00000260665.11:c.2461T= ENSP00000260665.7:p.Ser821=
NM_133259.3:c.2461T= NP_573566.2:p.Ser821=
XM_006711915.2:c.2383T= XP_006711978.1:p.Ser795=
XM_006711916.2:c.2461T= XP_006711979.1:p.Ser821=
XM_011532473.1:c.2461T= XP_011530775.1:p.Ser821=
XM_011532474.1:c.2461T= XP_011530776.1:p.Ser821=
XM_006711916.3:c.2461T= XP_006711979.1:p.Ser821=
XM_017003117.1:c.2383T= XP_016858606.1:p.Ser795=
XR_002958896.1:n.2503T=
NM_133259.4:c.2461T= MANE Select NP_573566.2:p.Ser821=