Canonical Allele Identifier: CA2493981250
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43905735G= , CM000664.2:g.43905735G= GRCh38
NC_000002.11:g.44132874G= , CM000664.1:g.44132874G= GRCh37
NC_000002.10:g.43986378G= NCBI36
NG_008247.1:g.95271C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000472420.6:n.400C=
ENST00000681993.1:n.873C=
ENST00000682295.1:c.476C= ENSP00000507499.1:n.476C=
ENST00000682303.1:c.*3107C= ENSP00000508325.1:n.*3107C=
ENST00000682308.1:c.3321C= ENSP00000507056.1:p.Asn1107=
ENST00000682480.1:c.3339C= ENSP00000508344.1:p.Asn1113=
ENST00000682546.1:c.3318C= ENSP00000508188.1:p.Asn1106=
ENST00000682585.1:c.3321C= ENSP00000506885.1:p.Asn1107=
ENST00000682595.1:n.3905C=
ENST00000682607.1:c.1739C=
ENST00000682612.1:c.173C=
ENST00000682779.1:c.3312C= ENSP00000507947.1:p.Asn1104=
ENST00000682845.1:n.2423C=
ENST00000682885.1:c.3276C= ENSP00000508036.1:p.Asn1092=
ENST00000682933.1:n.3395C=
ENST00000683002.1:c.173C=
ENST00000683072.1:n.3905C=
ENST00000683080.1:n.940C=
ENST00000683125.1:c.3429C= ENSP00000507939.1:p.Asn1143=
ENST00000683213.1:c.3324C= ENSP00000507751.1:p.Asn1108=
ENST00000683220.1:c.3351C= ENSP00000507151.1:p.Asn1117=
ENST00000683329.1:n.4124C=
ENST00000683346.1:c.*3196C= ENSP00000507458.1:n.*3196C=
ENST00000683409.1:n.1928C=
ENST00000683459.1:n.3908C=
ENST00000683528.1:c.173C=
ENST00000683590.1:c.3069C= ENSP00000506820.1:p.Asn1023=
ENST00000683623.1:c.3228C= ENSP00000507702.1:p.Asn1076=
ENST00000683645.1:n.3872C=
ENST00000683796.1:c.*3193C= ENSP00000508221.1:n.*3193C=
ENST00000683802.1:n.6246C=
ENST00000683833.1:c.3312C= ENSP00000506852.1:p.Asn1104=
ENST00000683994.1:c.3321C= ENSP00000507181.1:p.Asn1107=
ENST00000684290.1:c.*857C= ENSP00000507243.1:n.*857C=
ENST00000684306.1:c.*3234C= ENSP00000508384.1:n.*3234C=
ENST00000684341.1:n.3341C=
ENST00000684383.1:c.*2959C= ENSP00000506863.1:n.*2959C=
ENST00000684418.1:n.4502C=
ENST00000684454.1:n.2671C=
ENST00000684619.1:c.*3193C= ENSP00000508088.1:n.*3193C=
ENST00000684743.1:n.4352C=
ENST00000260665.12:c.3321C= MANE Select ENSP00000260665.7:p.Asn1107=
ENST00000260665.11:c.3321C= ENSP00000260665.7:p.Asn1107=
NM_133259.3:c.3321C= NP_573566.2:p.Asn1107=
XM_006711915.2:c.3243C= XP_006711978.1:p.Asn1081=
XM_011532473.1:c.3321C= XP_011530775.1:p.Asn1107=
XM_011532474.1:c.3321C= XP_011530776.1:p.Asn1107=
XM_017003117.1:c.3243C= XP_016858606.1:p.Asn1081=
XR_002958896.1:n.3363C=
NM_133259.4:c.3321C= MANE Select NP_573566.2:p.Asn1107=