Canonical Allele Identifier: CA2493977958
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43899325A= , CM000664.2:g.43899325A= GRCh38
NC_000002.11:g.44126464A= , CM000664.1:g.44126464A= GRCh37
NC_000002.10:g.43979968A= NCBI36
NG_008247.1:g.101681T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000419884.6:c.150T=
ENST00000472420.6:n.798T=
ENST00000483489.2:n.150T=
ENST00000681993.1:n.1271T=
ENST00000682303.1:c.*3505T= ENSP00000508325.1:n.*3505T=
ENST00000682308.1:c.3719T= ENSP00000507056.1:p.Met1240=
ENST00000682434.1:n.1270T=
ENST00000682480.1:c.3737T= ENSP00000508344.1:p.Met1246=
ENST00000682546.1:c.3716T= ENSP00000508188.1:p.Met1239=
ENST00000682585.1:c.3719T= ENSP00000506885.1:p.Met1240=
ENST00000682595.1:n.4303T=
ENST00000682607.1:c.2137T=
ENST00000682612.1:c.571T=
ENST00000682779.1:c.3710T= ENSP00000507947.1:p.Met1237=
ENST00000682845.1:n.2821T=
ENST00000682885.1:c.3674T= ENSP00000508036.1:p.Met1225=
ENST00000682933.1:n.3793T=
ENST00000683002.1:c.571T=
ENST00000683072.1:n.4303T=
ENST00000683080.1:n.1338T=
ENST00000683125.1:c.3827T= ENSP00000507939.1:p.Met1276=
ENST00000683213.1:c.3722T= ENSP00000507751.1:p.Met1241=
ENST00000683220.1:c.3749T= ENSP00000507151.1:p.Met1250=
ENST00000683329.1:n.4522T=
ENST00000683346.1:c.*3594T= ENSP00000507458.1:n.*3594T=
ENST00000683409.1:n.2326T=
ENST00000683459.1:n.4306T=
ENST00000683528.1:c.647T=
ENST00000683590.1:c.3467T= ENSP00000506820.1:p.Met1156=
ENST00000683623.1:c.3626T= ENSP00000507702.1:p.Met1209=
ENST00000683645.1:n.4270T=
ENST00000683796.1:c.*3591T= ENSP00000508221.1:n.*3591T=
ENST00000683802.1:n.6644T=
ENST00000683833.1:c.3710T= ENSP00000506852.1:p.Met1237=
ENST00000683994.1:c.3719T= ENSP00000507181.1:p.Met1240=
ENST00000684290.1:c.*1255T= ENSP00000507243.1:n.*1255T=
ENST00000684306.1:c.*3632T= ENSP00000508384.1:n.*3632T=
ENST00000684341.1:n.3739T=
ENST00000684383.1:c.*3357T= ENSP00000506863.1:n.*3357T=
ENST00000684418.1:n.4900T=
ENST00000684433.1:n.103T=
ENST00000684454.1:n.3069T=
ENST00000684619.1:c.*3591T= ENSP00000508088.1:n.*3591T=
ENST00000684743.1:n.6464T=
ENST00000260665.12:c.3719T= MANE Select ENSP00000260665.7:p.Met1240=
ENST00000260665.11:c.3719T= ENSP00000260665.7:p.Met1240=
ENST00000463456.5:n.2762T=
ENST00000472420.5:n.116T=
ENST00000483489.1:n.193T=
NM_133259.3:c.3719T= NP_573566.2:p.Met1240=
XM_006711915.2:c.3641T= XP_006711978.1:p.Met1214=
XM_011532473.1:c.3719T= XP_011530775.1:p.Met1240=
XM_011532474.1:c.3719T= XP_011530776.1:p.Met1240=
XM_017003117.1:c.3641T= XP_016858606.1:p.Met1214=
XR_002958896.1:n.3761T=
NM_133259.4:c.3719T= MANE Select NP_573566.2:p.Met1240=