Canonical Allele Identifier: CA425908210

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44132868G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43905729G>T , CM000664.2:g.43905729G>T	GRCh38
NC_000002.11:g.44132868G>T , CM000664.1:g.44132868G>T	GRCh37
NC_000002.10:g.43986372G>T	NCBI36
NG_008247.1:g.95277C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472420.6:n.406C>A
ENST00000681993.1:n.879C>A
ENST00000682295.1:c.482C>A	ENSP00000507499.1:n.482C>A
ENST00000682303.1:c.*3113C>A	ENSP00000508325.1:n.*3113C>A
ENST00000682308.1:c.3327C>A	ENSP00000507056.1:p.Arg1109=
ENST00000682480.1:c.3345C>A	ENSP00000508344.1:p.Arg1115=
ENST00000682546.1:c.3324C>A	ENSP00000508188.1:p.Arg1108=
ENST00000682585.1:c.3327C>A	ENSP00000506885.1:p.Arg1109=
ENST00000682595.1:n.3911C>A
ENST00000682607.1:c.1745C>A
ENST00000682612.1:c.179C>A
ENST00000682779.1:c.3318C>A	ENSP00000507947.1:p.Arg1106=
ENST00000682845.1:n.2429C>A
ENST00000682885.1:c.3282C>A	ENSP00000508036.1:p.Arg1094=
ENST00000682933.1:n.3401C>A
ENST00000683002.1:c.179C>A
ENST00000683072.1:n.3911C>A
ENST00000683080.1:n.946C>A
ENST00000683125.1:c.3435C>A	ENSP00000507939.1:p.Arg1145=
ENST00000683213.1:c.3330C>A	ENSP00000507751.1:p.Arg1110=
ENST00000683220.1:c.3357C>A	ENSP00000507151.1:p.Arg1119=
ENST00000683329.1:n.4130C>A
ENST00000683346.1:c.*3202C>A	ENSP00000507458.1:n.*3202C>A
ENST00000683409.1:n.1934C>A
ENST00000683459.1:n.3914C>A
ENST00000683528.1:c.179C>A
ENST00000683590.1:c.3075C>A	ENSP00000506820.1:p.Arg1025=
ENST00000683623.1:c.3234C>A	ENSP00000507702.1:p.Arg1078=
ENST00000683645.1:n.3878C>A
ENST00000683796.1:c.*3199C>A	ENSP00000508221.1:n.*3199C>A
ENST00000683802.1:n.6252C>A
ENST00000683833.1:c.3318C>A	ENSP00000506852.1:p.Arg1106=
ENST00000683994.1:c.3327C>A	ENSP00000507181.1:p.Arg1109=
ENST00000684290.1:c.*863C>A	ENSP00000507243.1:n.*863C>A
ENST00000684306.1:c.*3240C>A	ENSP00000508384.1:n.*3240C>A
ENST00000684341.1:n.3347C>A
ENST00000684383.1:c.*2965C>A	ENSP00000506863.1:n.*2965C>A
ENST00000684418.1:n.4508C>A
ENST00000684454.1:n.2677C>A
ENST00000684619.1:c.*3199C>A	ENSP00000508088.1:n.*3199C>A
ENST00000684743.1:n.4358C>A
ENST00000260665.12:c.3327C>A MANE Select	ENSP00000260665.7:p.Arg1109=
ENST00000260665.11:c.3327C>A	ENSP00000260665.7:p.Arg1109=
NM_133259.3:c.3327C>A	NP_573566.2:p.Arg1109=
XM_006711915.2:c.3249C>A	XP_006711978.1:p.Arg1083=
XM_011532473.1:c.3327C>A	XP_011530775.1:p.Arg1109=
XM_011532474.1:c.3327C>A	XP_011530776.1:p.Arg1109=
XM_017003117.1:c.3249C>A	XP_016858606.1:p.Arg1083=
XR_002958896.1:n.3369C>A
NM_133259.4:c.3327C>A MANE Select	NP_573566.2:p.Arg1109=