Canonical Allele Identifier: CA2493988105
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43918080T= , CM000664.2:g.43918080T= GRCh38
NC_000002.11:g.44145219T= , CM000664.1:g.44145219T= GRCh37
NC_000002.10:g.43998723T= NCBI36
NG_008247.1:g.82926A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681993.1:n.645A=
ENST00000682295.1:c.303+176A= ENSP00000507499.1:n.303+176A=
ENST00000682303.1:c.*2879A= ENSP00000508325.1:n.*2879A=
ENST00000682308.1:c.3093A= ENSP00000507056.1:p.Thr1031=
ENST00000682480.1:c.3111A= ENSP00000508344.1:p.Thr1037=
ENST00000682546.1:c.3090A= ENSP00000508188.1:p.Thr1030=
ENST00000682585.1:c.3093A= ENSP00000506885.1:p.Thr1031=
ENST00000682595.1:n.3677A=
ENST00000682607.1:c.1511A=
ENST00000682779.1:c.3084A= ENSP00000507947.1:p.Thr1028=
ENST00000682845.1:n.2195A=
ENST00000682885.1:c.3048A= ENSP00000508036.1:p.Thr1016=
ENST00000682933.1:n.3167A=
ENST00000683072.1:n.3677A=
ENST00000683080.1:n.712A=
ENST00000683125.1:c.3201A= ENSP00000507939.1:p.Thr1067=
ENST00000683213.1:c.3096A= ENSP00000507751.1:p.Thr1032=
ENST00000683220.1:c.3123A= ENSP00000507151.1:p.Thr1041=
ENST00000683329.1:n.3896A=
ENST00000683346.1:c.*2968A= ENSP00000507458.1:n.*2968A=
ENST00000683409.1:n.1700A=
ENST00000683459.1:n.3680A=
ENST00000683590.1:c.2897-5522A= ENSP00000506820.1:n.2897-5522A=
ENST00000683623.1:c.3000A= ENSP00000507702.1:p.Thr1000=
ENST00000683645.1:n.3644A=
ENST00000683796.1:c.*2965A= ENSP00000508221.1:n.*2965A=
ENST00000683802.1:n.6018A=
ENST00000683833.1:c.3084A= ENSP00000506852.1:p.Thr1028=
ENST00000683994.1:c.3093A= ENSP00000507181.1:p.Thr1031=
ENST00000684290.1:c.*629A= ENSP00000507243.1:n.*629A=
ENST00000684306.1:c.*3006A= ENSP00000508384.1:n.*3006A=
ENST00000684341.1:n.3113A=
ENST00000684383.1:c.*2731A= ENSP00000506863.1:n.*2731A=
ENST00000684619.1:c.*2965A= ENSP00000508088.1:n.*2965A=
ENST00000684705.1:n.214A=
ENST00000684743.1:n.4124A=
ENST00000260665.12:c.3093A= MANE Select ENSP00000260665.7:p.Thr1031=
ENST00000260665.11:c.3093A= ENSP00000260665.7:p.Thr1031=
NM_133259.3:c.3093A= NP_573566.2:p.Thr1031=
XM_006711915.2:c.3015A= XP_006711978.1:p.Thr1005=
XM_006711916.2:c.3093A= XP_006711979.1:p.Thr1031=
XM_011532473.1:c.3093A= XP_011530775.1:p.Thr1031=
XM_011532474.1:c.3093A= XP_011530776.1:p.Thr1031=
XM_006711916.3:c.3093A= XP_006711979.1:p.Thr1031=
XM_017003117.1:c.3015A= XP_016858606.1:p.Thr1005=
XR_002958896.1:n.3135A=
NM_133259.4:c.3093A= MANE Select NP_573566.2:p.Thr1031=