Canonical Allele Identifier: CA2493977953
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43899313A= , CM000664.2:g.43899313A= GRCh38
NC_000002.11:g.44126452A= , CM000664.1:g.44126452A= GRCh37
NC_000002.10:g.43979956A= NCBI36
NG_008247.1:g.101693T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000419884.6:c.162T=
ENST00000472420.6:n.810T=
ENST00000483489.2:n.162T=
ENST00000681993.1:n.1283T=
ENST00000682303.1:c.*3517T= ENSP00000508325.1:n.*3517T=
ENST00000682308.1:c.3731T= ENSP00000507056.1:p.Leu1244=
ENST00000682434.1:n.1282T=
ENST00000682480.1:c.3749T= ENSP00000508344.1:p.Leu1250=
ENST00000682546.1:c.3728T= ENSP00000508188.1:p.Leu1243=
ENST00000682585.1:c.3731T= ENSP00000506885.1:p.Leu1244=
ENST00000682595.1:n.4315T=
ENST00000682607.1:c.2149T=
ENST00000682612.1:c.583T=
ENST00000682779.1:c.3722T= ENSP00000507947.1:p.Leu1241=
ENST00000682845.1:n.2833T=
ENST00000682885.1:c.3686T= ENSP00000508036.1:p.Leu1229=
ENST00000682933.1:n.3805T=
ENST00000683002.1:c.583T=
ENST00000683072.1:n.4315T=
ENST00000683080.1:n.1350T=
ENST00000683125.1:c.3839T= ENSP00000507939.1:p.Leu1280=
ENST00000683213.1:c.3734T= ENSP00000507751.1:p.Leu1245=
ENST00000683220.1:c.3761T= ENSP00000507151.1:p.Leu1254=
ENST00000683329.1:n.4534T=
ENST00000683346.1:c.*3606T= ENSP00000507458.1:n.*3606T=
ENST00000683409.1:n.2338T=
ENST00000683459.1:n.4318T=
ENST00000683528.1:c.659T=
ENST00000683590.1:c.3479T= ENSP00000506820.1:p.Leu1160=
ENST00000683623.1:c.3638T= ENSP00000507702.1:p.Leu1213=
ENST00000683645.1:n.4282T=
ENST00000683796.1:c.*3603T= ENSP00000508221.1:n.*3603T=
ENST00000683802.1:n.6656T=
ENST00000683833.1:c.3722T= ENSP00000506852.1:p.Leu1241=
ENST00000683994.1:c.3731T= ENSP00000507181.1:p.Leu1244=
ENST00000684290.1:c.*1267T= ENSP00000507243.1:n.*1267T=
ENST00000684306.1:c.*3644T= ENSP00000508384.1:n.*3644T=
ENST00000684341.1:n.3751T=
ENST00000684383.1:c.*3369T= ENSP00000506863.1:n.*3369T=
ENST00000684418.1:n.4912T=
ENST00000684433.1:n.115T=
ENST00000684454.1:n.3081T=
ENST00000684619.1:c.*3603T= ENSP00000508088.1:n.*3603T=
ENST00000684743.1:n.6476T=
ENST00000260665.12:c.3731T= MANE Select ENSP00000260665.7:p.Leu1244=
ENST00000260665.11:c.3731T= ENSP00000260665.7:p.Leu1244=
ENST00000463456.5:n.2774T=
ENST00000472420.5:n.128T=
ENST00000483489.1:n.205T=
NM_133259.3:c.3731T= NP_573566.2:p.Leu1244=
XM_006711915.2:c.3653T= XP_006711978.1:p.Leu1218=
XM_011532473.1:c.3731T= XP_011530775.1:p.Leu1244=
XM_011532474.1:c.3731T= XP_011530776.1:p.Leu1244=
XM_017003117.1:c.3653T= XP_016858606.1:p.Leu1218=
XR_002958896.1:n.3773T=
NM_133259.4:c.3731T= MANE Select NP_573566.2:p.Leu1244=