Canonical Allele Identifier: CA2493981253
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43905742G= , CM000664.2:g.43905742G= GRCh38
NC_000002.11:g.44132881G= , CM000664.1:g.44132881G= GRCh37
NC_000002.10:g.43986385G= NCBI36
NG_008247.1:g.95264C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000472420.6:n.393C=
ENST00000681993.1:n.866C=
ENST00000682295.1:c.469C= ENSP00000507499.1:n.469C=
ENST00000682303.1:c.*3100C= ENSP00000508325.1:n.*3100C=
ENST00000682308.1:c.3314C= ENSP00000507056.1:p.Ala1105=
ENST00000682480.1:c.3332C= ENSP00000508344.1:p.Ala1111=
ENST00000682546.1:c.3311C= ENSP00000508188.1:p.Ala1104=
ENST00000682585.1:c.3314C= ENSP00000506885.1:p.Ala1105=
ENST00000682595.1:n.3898C=
ENST00000682607.1:c.1732C=
ENST00000682612.1:c.166C=
ENST00000682779.1:c.3305C= ENSP00000507947.1:p.Ala1102=
ENST00000682845.1:n.2416C=
ENST00000682885.1:c.3269C= ENSP00000508036.1:p.Ala1090=
ENST00000682933.1:n.3388C=
ENST00000683002.1:c.166C=
ENST00000683072.1:n.3898C=
ENST00000683080.1:n.933C=
ENST00000683125.1:c.3422C= ENSP00000507939.1:p.Ala1141=
ENST00000683213.1:c.3317C= ENSP00000507751.1:p.Ala1106=
ENST00000683220.1:c.3344C= ENSP00000507151.1:p.Ala1115=
ENST00000683329.1:n.4117C=
ENST00000683346.1:c.*3189C= ENSP00000507458.1:n.*3189C=
ENST00000683409.1:n.1921C=
ENST00000683459.1:n.3901C=
ENST00000683528.1:c.166C=
ENST00000683590.1:c.3062C= ENSP00000506820.1:p.Ala1021=
ENST00000683623.1:c.3221C= ENSP00000507702.1:p.Ala1074=
ENST00000683645.1:n.3865C=
ENST00000683796.1:c.*3186C= ENSP00000508221.1:n.*3186C=
ENST00000683802.1:n.6239C=
ENST00000683833.1:c.3305C= ENSP00000506852.1:p.Ala1102=
ENST00000683994.1:c.3314C= ENSP00000507181.1:p.Ala1105=
ENST00000684290.1:c.*850C= ENSP00000507243.1:n.*850C=
ENST00000684306.1:c.*3227C= ENSP00000508384.1:n.*3227C=
ENST00000684341.1:n.3334C=
ENST00000684383.1:c.*2952C= ENSP00000506863.1:n.*2952C=
ENST00000684418.1:n.4495C=
ENST00000684454.1:n.2664C=
ENST00000684619.1:c.*3186C= ENSP00000508088.1:n.*3186C=
ENST00000684743.1:n.4345C=
ENST00000260665.12:c.3314C= MANE Select ENSP00000260665.7:p.Ala1105=
ENST00000260665.11:c.3314C= ENSP00000260665.7:p.Ala1105=
NM_133259.3:c.3314C= NP_573566.2:p.Ala1105=
XM_006711915.2:c.3236C= XP_006711978.1:p.Ala1079=
XM_011532473.1:c.3314C= XP_011530775.1:p.Ala1105=
XM_011532474.1:c.3314C= XP_011530776.1:p.Ala1105=
XM_017003117.1:c.3236C= XP_016858606.1:p.Ala1079=
XR_002958896.1:n.3356C=
NM_133259.4:c.3314C= MANE Select NP_573566.2:p.Ala1105=