Canonical Allele Identifier: CA2493977935
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43899270G= , CM000664.2:g.43899270G= GRCh38
NC_000002.11:g.44126409G= , CM000664.1:g.44126409G= GRCh37
NC_000002.10:g.43979913G= NCBI36
NG_008247.1:g.101736C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000419884.6:c.205C=
ENST00000472420.6:n.853C=
ENST00000483489.2:n.205C=
ENST00000681993.1:n.1326C=
ENST00000682303.1:c.*3560C= ENSP00000508325.1:n.*3560C=
ENST00000682308.1:c.3774C= ENSP00000507056.1:p.Phe1258=
ENST00000682434.1:n.1325C=
ENST00000682480.1:c.3792C= ENSP00000508344.1:p.Phe1264=
ENST00000682546.1:c.3771C= ENSP00000508188.1:p.Phe1257=
ENST00000682585.1:c.3774C= ENSP00000506885.1:p.Phe1258=
ENST00000682595.1:n.4358C=
ENST00000682607.1:c.2192C=
ENST00000682612.1:c.626C=
ENST00000682779.1:c.3765C= ENSP00000507947.1:p.Phe1255=
ENST00000682845.1:n.2876C=
ENST00000682885.1:c.3729C= ENSP00000508036.1:p.Phe1243=
ENST00000682933.1:n.3848C=
ENST00000683002.1:c.626C=
ENST00000683072.1:n.4358C=
ENST00000683080.1:n.1393C=
ENST00000683125.1:c.3882C= ENSP00000507939.1:p.Phe1294=
ENST00000683213.1:c.3777C= ENSP00000507751.1:p.Phe1259=
ENST00000683220.1:c.3804C= ENSP00000507151.1:p.Phe1268=
ENST00000683329.1:n.4577C=
ENST00000683346.1:c.*3649C= ENSP00000507458.1:n.*3649C=
ENST00000683409.1:n.2381C=
ENST00000683459.1:n.4361C=
ENST00000683528.1:c.702C=
ENST00000683590.1:c.3522C= ENSP00000506820.1:p.Phe1174=
ENST00000683623.1:c.3681C= ENSP00000507702.1:p.Phe1227=
ENST00000683645.1:n.4325C=
ENST00000683796.1:c.*3646C= ENSP00000508221.1:n.*3646C=
ENST00000683802.1:n.6699C=
ENST00000683833.1:c.3765C= ENSP00000506852.1:p.Phe1255=
ENST00000683994.1:c.3774C= ENSP00000507181.1:p.Phe1258=
ENST00000684290.1:c.*1310C= ENSP00000507243.1:n.*1310C=
ENST00000684306.1:c.*3687C= ENSP00000508384.1:n.*3687C=
ENST00000684341.1:n.3794C=
ENST00000684383.1:c.*3412C= ENSP00000506863.1:n.*3412C=
ENST00000684418.1:n.4955C=
ENST00000684433.1:n.158C=
ENST00000684454.1:n.3124C=
ENST00000684619.1:c.*3646C= ENSP00000508088.1:n.*3646C=
ENST00000684743.1:n.6519C=
ENST00000260665.12:c.3774C= MANE Select ENSP00000260665.7:p.Phe1258=
ENST00000260665.11:c.3774C= ENSP00000260665.7:p.Phe1258=
ENST00000419884.5:c.15C= ENSP00000414207.1:p.Phe5=
ENST00000463456.5:n.2817C=
ENST00000472420.5:n.171C=
ENST00000483489.1:n.248C=
NM_133259.3:c.3774C= NP_573566.2:p.Phe1258=
XM_006711915.2:c.3696C= XP_006711978.1:p.Phe1232=
XM_011532473.1:c.3774C= XP_011530775.1:p.Phe1258=
XM_011532474.1:c.3774C= XP_011530776.1:p.Phe1258=
XM_017003117.1:c.3696C= XP_016858606.1:p.Phe1232=
XR_002958896.1:n.3816C=
NM_133259.4:c.3774C= MANE Select NP_573566.2:p.Phe1258=