Canonical Allele Identifier: CA2493988253
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43918394T= , CM000664.2:g.43918394T= GRCh38
NC_000002.11:g.44145533T= , CM000664.1:g.44145533T= GRCh37
NC_000002.10:g.43999037T= NCBI36
NG_008247.1:g.82612A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681993.1:n.453A=
ENST00000682295.1:c.165A= ENSP00000507499.1:p.Ile55=
ENST00000682303.1:c.*2687A= ENSP00000508325.1:n.*2687A=
ENST00000682308.1:c.2901A= ENSP00000507056.1:p.Ile967=
ENST00000682480.1:c.2901A= ENSP00000508344.1:p.Ile967=
ENST00000682546.1:c.2898A= ENSP00000508188.1:p.Ile966=
ENST00000682585.1:c.2901A= ENSP00000506885.1:p.Ile967=
ENST00000682595.1:n.3485A=
ENST00000682607.1:c.1319A=
ENST00000682779.1:c.2892A= ENSP00000507947.1:p.Ile964=
ENST00000682845.1:n.2003A=
ENST00000682885.1:c.2856A= ENSP00000508036.1:p.Ile952=
ENST00000682933.1:n.2975A=
ENST00000683072.1:n.3485A=
ENST00000683080.1:n.520A=
ENST00000683125.1:c.3009A= ENSP00000507939.1:p.Ile1003=
ENST00000683213.1:c.2904A= ENSP00000507751.1:p.Ile968=
ENST00000683220.1:c.2931A= ENSP00000507151.1:p.Ile977=
ENST00000683236.1:c.231A= ENSP00000506891.1:n.231A=
ENST00000683329.1:n.3704A=
ENST00000683346.1:c.*2776A= ENSP00000507458.1:n.*2776A=
ENST00000683409.1:n.1508A=
ENST00000683459.1:n.3488A=
ENST00000683590.1:c.2897-5836A= ENSP00000506820.1:n.2897-5836A=
ENST00000683623.1:c.2808A= ENSP00000507702.1:p.Ile936=
ENST00000683645.1:n.3452A=
ENST00000683796.1:c.*2773A= ENSP00000508221.1:n.*2773A=
ENST00000683802.1:n.5826A=
ENST00000683833.1:c.2892A= ENSP00000506852.1:p.Ile964=
ENST00000683994.1:c.2901A= ENSP00000507181.1:p.Ile967=
ENST00000684290.1:c.*437A= ENSP00000507243.1:n.*437A=
ENST00000684306.1:c.*2814A= ENSP00000508384.1:n.*2814A=
ENST00000684341.1:n.2921A=
ENST00000684383.1:c.*2539A= ENSP00000506863.1:n.*2539A=
ENST00000684619.1:c.*2773A= ENSP00000508088.1:n.*2773A=
ENST00000684705.1:n.22A=
ENST00000684743.1:n.3932A=
ENST00000260665.12:c.2901A= MANE Select ENSP00000260665.7:p.Ile967=
ENST00000260665.11:c.2901A= ENSP00000260665.7:p.Ile967=
NM_133259.3:c.2901A= NP_573566.2:p.Ile967=
XM_006711915.2:c.2823A= XP_006711978.1:p.Ile941=
XM_006711916.2:c.2901A= XP_006711979.1:p.Ile967=
XM_011532473.1:c.2901A= XP_011530775.1:p.Ile967=
XM_011532474.1:c.2901A= XP_011530776.1:p.Ile967=
XM_006711916.3:c.2901A= XP_006711979.1:p.Ile967=
XM_017003117.1:c.2823A= XP_016858606.1:p.Ile941=
XR_002958896.1:n.2943A=
NM_133259.4:c.2901A= MANE Select NP_573566.2:p.Ile967=