Canonical Allele Identifier: CA425909743

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44170921T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43943782T>C , CM000664.2:g.43943782T>C	GRCh38
NC_000002.11:g.44170921T>C , CM000664.1:g.44170921T>C	GRCh37
NC_000002.10:g.44024425T>C	NCBI36
NG_008247.1:g.57224A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000409659.6:c.2409A>G	ENSP00000386562.2:p.Glu803=
ENST00000447246.2:c.2409A>G	ENSP00000403637.2:p.Glu803=
ENST00000681961.1:n.2429A>G
ENST00000682104.1:c.2283A>G	ENSP00000507716.1:p.Glu761=
ENST00000682303.1:c.*2195A>G	ENSP00000508325.1:n.*2195A>G
ENST00000682308.1:c.2409A>G	ENSP00000507056.1:p.Glu803=
ENST00000682480.1:c.2409A>G	ENSP00000508344.1:p.Glu803=
ENST00000682546.1:c.2406A>G	ENSP00000508188.1:p.Glu802=
ENST00000682585.1:c.2409A>G	ENSP00000506885.1:p.Glu803=
ENST00000682595.1:n.2991A>G
ENST00000682607.1:c.827A>G
ENST00000682779.1:c.2400A>G	ENSP00000507947.1:p.Glu800=
ENST00000682845.1:n.1511A>G
ENST00000682885.1:c.2364A>G	ENSP00000508036.1:p.Glu788=
ENST00000682933.1:n.2483A>G
ENST00000683072.1:n.2991A>G
ENST00000683125.1:c.2409A>G	ENSP00000507939.1:p.Glu803=
ENST00000683213.1:c.2412A>G	ENSP00000507751.1:p.Glu804=
ENST00000683220.1:c.2439A>G	ENSP00000507151.1:p.Glu813=
ENST00000683329.1:n.3212A>G
ENST00000683346.1:c.*2284A>G	ENSP00000507458.1:n.*2284A>G
ENST00000683459.1:n.2996A>G
ENST00000683590.1:c.2409A>G	ENSP00000506820.1:p.Glu803=
ENST00000683623.1:c.2316A>G	ENSP00000507702.1:p.Glu772=
ENST00000683645.1:n.2960A>G
ENST00000683694.1:n.1160A>G
ENST00000683796.1:c.*2281A>G	ENSP00000508221.1:n.*2281A>G
ENST00000683802.1:n.5334A>G
ENST00000683833.1:c.2400A>G	ENSP00000506852.1:p.Glu800=
ENST00000683989.1:c.2409A>G	ENSP00000507510.1:p.Glu803=
ENST00000683994.1:c.2409A>G	ENSP00000507181.1:p.Glu803=
ENST00000684290.1:c.*103A>G	ENSP00000507243.1:n.*103A>G
ENST00000684306.1:c.*2322A>G	ENSP00000508384.1:n.*2322A>G
ENST00000684341.1:n.2429A>G
ENST00000684383.1:c.*2047A>G	ENSP00000506863.1:n.*2047A>G
ENST00000684397.1:c.113A>G
ENST00000684619.1:c.*2281A>G	ENSP00000508088.1:n.*2281A>G
ENST00000684743.1:n.3440A>G
ENST00000260665.12:c.2409A>G MANE Select	ENSP00000260665.7:p.Glu803=
ENST00000260665.11:c.2409A>G	ENSP00000260665.7:p.Glu803=
NM_133259.3:c.2409A>G	NP_573566.2:p.Glu803=
XM_006711915.2:c.2331A>G	XP_006711978.1:p.Glu777=
XM_006711916.2:c.2409A>G	XP_006711979.1:p.Glu803=
XM_011532473.1:c.2409A>G	XP_011530775.1:p.Glu803=
XM_011532474.1:c.2409A>G	XP_011530776.1:p.Glu803=
XM_006711916.3:c.2409A>G	XP_006711979.1:p.Glu803=
XM_017003117.1:c.2331A>G	XP_016858606.1:p.Glu777=
XR_002958896.1:n.2451A>G
NM_133259.4:c.2409A>G MANE Select	NP_573566.2:p.Glu803=