Canonical Allele Identifier: CA2493988236
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43918363A= , CM000664.2:g.43918363A= GRCh38
NC_000002.11:g.44145502A= , CM000664.1:g.44145502A= GRCh37
NC_000002.10:g.43999006A= NCBI36
NG_008247.1:g.82643T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681993.1:n.484T=
ENST00000682295.1:c.196T= ENSP00000507499.1:p.Trp66=
ENST00000682303.1:c.*2718T= ENSP00000508325.1:n.*2718T=
ENST00000682308.1:c.2932T= ENSP00000507056.1:p.Trp978=
ENST00000682480.1:c.2932T= ENSP00000508344.1:p.Trp978=
ENST00000682546.1:c.2929T= ENSP00000508188.1:p.Trp977=
ENST00000682585.1:c.2932T= ENSP00000506885.1:p.Trp978=
ENST00000682595.1:n.3516T=
ENST00000682607.1:c.1350T=
ENST00000682779.1:c.2923T= ENSP00000507947.1:p.Trp975=
ENST00000682845.1:n.2034T=
ENST00000682885.1:c.2887T= ENSP00000508036.1:p.Trp963=
ENST00000682933.1:n.3006T=
ENST00000683072.1:n.3516T=
ENST00000683080.1:n.551T=
ENST00000683125.1:c.3040T= ENSP00000507939.1:p.Trp1014=
ENST00000683213.1:c.2935T= ENSP00000507751.1:p.Trp979=
ENST00000683220.1:c.2962T= ENSP00000507151.1:p.Trp988=
ENST00000683236.1:c.262T= ENSP00000506891.1:n.262T=
ENST00000683329.1:n.3735T=
ENST00000683346.1:c.*2807T= ENSP00000507458.1:n.*2807T=
ENST00000683409.1:n.1539T=
ENST00000683459.1:n.3519T=
ENST00000683590.1:c.2897-5805T= ENSP00000506820.1:n.2897-5805T=
ENST00000683623.1:c.2839T= ENSP00000507702.1:p.Trp947=
ENST00000683645.1:n.3483T=
ENST00000683796.1:c.*2804T= ENSP00000508221.1:n.*2804T=
ENST00000683802.1:n.5857T=
ENST00000683833.1:c.2923T= ENSP00000506852.1:p.Trp975=
ENST00000683994.1:c.2932T= ENSP00000507181.1:p.Trp978=
ENST00000684290.1:c.*468T= ENSP00000507243.1:n.*468T=
ENST00000684306.1:c.*2845T= ENSP00000508384.1:n.*2845T=
ENST00000684341.1:n.2952T=
ENST00000684383.1:c.*2570T= ENSP00000506863.1:n.*2570T=
ENST00000684619.1:c.*2804T= ENSP00000508088.1:n.*2804T=
ENST00000684705.1:n.53T=
ENST00000684743.1:n.3963T=
ENST00000260665.12:c.2932T= MANE Select ENSP00000260665.7:p.Trp978=
ENST00000260665.11:c.2932T= ENSP00000260665.7:p.Trp978=
NM_133259.3:c.2932T= NP_573566.2:p.Trp978=
XM_006711915.2:c.2854T= XP_006711978.1:p.Trp952=
XM_006711916.2:c.2932T= XP_006711979.1:p.Trp978=
XM_011532473.1:c.2932T= XP_011530775.1:p.Trp978=
XM_011532474.1:c.2932T= XP_011530776.1:p.Trp978=
XM_006711916.3:c.2932T= XP_006711979.1:p.Trp978=
XM_017003117.1:c.2854T= XP_016858606.1:p.Trp952=
XR_002958896.1:n.2974T=
NM_133259.4:c.2932T= MANE Select NP_573566.2:p.Trp978=