Canonical Allele Identifier: CA2493988193
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43918268A= , CM000664.2:g.43918268A= GRCh38
NC_000002.11:g.44145407A= , CM000664.1:g.44145407A= GRCh37
NC_000002.10:g.43998911A= NCBI36
NG_008247.1:g.82738T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681993.1:n.579T=
ENST00000682295.1:c.291T= ENSP00000507499.1:p.Phe97=
ENST00000682303.1:c.*2813T= ENSP00000508325.1:n.*2813T=
ENST00000682308.1:c.3027T= ENSP00000507056.1:p.Phe1009=
ENST00000682480.1:c.3027T= ENSP00000508344.1:p.Phe1009=
ENST00000682546.1:c.3024T= ENSP00000508188.1:p.Phe1008=
ENST00000682585.1:c.3027T= ENSP00000506885.1:p.Phe1009=
ENST00000682595.1:n.3611T=
ENST00000682607.1:c.1445T=
ENST00000682779.1:c.3018T= ENSP00000507947.1:p.Phe1006=
ENST00000682845.1:n.2129T=
ENST00000682885.1:c.2982T= ENSP00000508036.1:p.Phe994=
ENST00000682933.1:n.3101T=
ENST00000683072.1:n.3611T=
ENST00000683080.1:n.646T=
ENST00000683125.1:c.3135T= ENSP00000507939.1:p.Phe1045=
ENST00000683213.1:c.3030T= ENSP00000507751.1:p.Phe1010=
ENST00000683220.1:c.3057T= ENSP00000507151.1:p.Phe1019=
ENST00000683236.1:c.357T= ENSP00000506891.1:n.357T=
ENST00000683329.1:n.3830T=
ENST00000683346.1:c.*2902T= ENSP00000507458.1:n.*2902T=
ENST00000683409.1:n.1634T=
ENST00000683459.1:n.3614T=
ENST00000683590.1:c.2897-5710T= ENSP00000506820.1:n.2897-5710T=
ENST00000683623.1:c.2934T= ENSP00000507702.1:p.Phe978=
ENST00000683645.1:n.3578T=
ENST00000683796.1:c.*2899T= ENSP00000508221.1:n.*2899T=
ENST00000683802.1:n.5952T=
ENST00000683833.1:c.3018T= ENSP00000506852.1:p.Phe1006=
ENST00000683994.1:c.3027T= ENSP00000507181.1:p.Phe1009=
ENST00000684290.1:c.*563T= ENSP00000507243.1:n.*563T=
ENST00000684306.1:c.*2940T= ENSP00000508384.1:n.*2940T=
ENST00000684341.1:n.3047T=
ENST00000684383.1:c.*2665T= ENSP00000506863.1:n.*2665T=
ENST00000684619.1:c.*2899T= ENSP00000508088.1:n.*2899T=
ENST00000684705.1:n.148T=
ENST00000684743.1:n.4058T=
ENST00000260665.12:c.3027T= MANE Select ENSP00000260665.7:p.Phe1009=
ENST00000260665.11:c.3027T= ENSP00000260665.7:p.Phe1009=
NM_133259.3:c.3027T= NP_573566.2:p.Phe1009=
XM_006711915.2:c.2949T= XP_006711978.1:p.Phe983=
XM_006711916.2:c.3027T= XP_006711979.1:p.Phe1009=
XM_011532473.1:c.3027T= XP_011530775.1:p.Phe1009=
XM_011532474.1:c.3027T= XP_011530776.1:p.Phe1009=
XM_006711916.3:c.3027T= XP_006711979.1:p.Phe1009=
XM_017003117.1:c.2949T= XP_016858606.1:p.Phe983=
XR_002958896.1:n.3069T=
NM_133259.4:c.3027T= MANE Select NP_573566.2:p.Phe1009=