Canonical Allele Identifier: CA2493981255
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43905746C= , CM000664.2:g.43905746C= GRCh38
NC_000002.11:g.44132885C= , CM000664.1:g.44132885C= GRCh37
NC_000002.10:g.43986389C= NCBI36
NG_008247.1:g.95260G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000472420.6:n.389G=
ENST00000681993.1:n.862G=
ENST00000682295.1:c.465G= ENSP00000507499.1:n.465G=
ENST00000682303.1:c.*3096G= ENSP00000508325.1:n.*3096G=
ENST00000682308.1:c.3310G= ENSP00000507056.1:p.Asp1104=
ENST00000682480.1:c.3328G= ENSP00000508344.1:p.Asp1110=
ENST00000682546.1:c.3307G= ENSP00000508188.1:p.Asp1103=
ENST00000682585.1:c.3310G= ENSP00000506885.1:p.Asp1104=
ENST00000682595.1:n.3894G=
ENST00000682607.1:c.1728G=
ENST00000682612.1:c.162G=
ENST00000682779.1:c.3301G= ENSP00000507947.1:p.Asp1101=
ENST00000682845.1:n.2412G=
ENST00000682885.1:c.3265G= ENSP00000508036.1:p.Asp1089=
ENST00000682933.1:n.3384G=
ENST00000683002.1:c.162G=
ENST00000683072.1:n.3894G=
ENST00000683080.1:n.929G=
ENST00000683125.1:c.3418G= ENSP00000507939.1:p.Asp1140=
ENST00000683213.1:c.3313G= ENSP00000507751.1:p.Asp1105=
ENST00000683220.1:c.3340G= ENSP00000507151.1:p.Asp1114=
ENST00000683329.1:n.4113G=
ENST00000683346.1:c.*3185G= ENSP00000507458.1:n.*3185G=
ENST00000683409.1:n.1917G=
ENST00000683459.1:n.3897G=
ENST00000683528.1:c.162G=
ENST00000683590.1:c.3058G= ENSP00000506820.1:p.Asp1020=
ENST00000683623.1:c.3217G= ENSP00000507702.1:p.Asp1073=
ENST00000683645.1:n.3861G=
ENST00000683796.1:c.*3182G= ENSP00000508221.1:n.*3182G=
ENST00000683802.1:n.6235G=
ENST00000683833.1:c.3301G= ENSP00000506852.1:p.Asp1101=
ENST00000683994.1:c.3310G= ENSP00000507181.1:p.Asp1104=
ENST00000684290.1:c.*846G= ENSP00000507243.1:n.*846G=
ENST00000684306.1:c.*3223G= ENSP00000508384.1:n.*3223G=
ENST00000684341.1:n.3330G=
ENST00000684383.1:c.*2948G= ENSP00000506863.1:n.*2948G=
ENST00000684418.1:n.4491G=
ENST00000684454.1:n.2660G=
ENST00000684619.1:c.*3182G= ENSP00000508088.1:n.*3182G=
ENST00000684743.1:n.4341G=
ENST00000260665.12:c.3310G= MANE Select ENSP00000260665.7:p.Asp1104=
ENST00000260665.11:c.3310G= ENSP00000260665.7:p.Asp1104=
NM_133259.3:c.3310G= NP_573566.2:p.Asp1104=
XM_006711915.2:c.3232G= XP_006711978.1:p.Asp1078=
XM_011532473.1:c.3310G= XP_011530775.1:p.Asp1104=
XM_011532474.1:c.3310G= XP_011530776.1:p.Asp1104=
XM_017003117.1:c.3232G= XP_016858606.1:p.Asp1078=
XR_002958896.1:n.3352G=
NM_133259.4:c.3310G= MANE Select NP_573566.2:p.Asp1104=