Canonical Allele Identifier: CA2494004295
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43948177A= , CM000664.2:g.43948177A= GRCh38
NC_000002.11:g.44175316A= , CM000664.1:g.44175316A= GRCh37
NC_000002.10:g.44028820A= NCBI36
NG_008247.1:g.52829T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409659.6:c.1865T= ENSP00000386562.2:p.Ile622=
ENST00000447246.2:c.1865T= ENSP00000403637.2:p.Ile622=
ENST00000467058.2:n.594T=
ENST00000681959.1:n.1479T=
ENST00000681961.1:n.1885T=
ENST00000682104.1:c.1739T= ENSP00000507716.1:p.Ile580=
ENST00000682303.1:c.*1737T= ENSP00000508325.1:n.*1737T=
ENST00000682308.1:c.1865T= ENSP00000507056.1:p.Ile622=
ENST00000682480.1:c.1865T= ENSP00000508344.1:p.Ile622=
ENST00000682546.1:c.1862T= ENSP00000508188.1:p.Ile621=
ENST00000682585.1:c.1865T= ENSP00000506885.1:p.Ile622=
ENST00000682595.1:n.2447T=
ENST00000682607.1:c.283T=
ENST00000682779.1:c.1856T= ENSP00000507947.1:p.Ile619=
ENST00000682885.1:c.1865T= ENSP00000508036.1:p.Ile622=
ENST00000682933.1:n.1939T=
ENST00000683072.1:n.2447T=
ENST00000683082.1:n.1883T=
ENST00000683125.1:c.1865T= ENSP00000507939.1:p.Ile622=
ENST00000683213.1:c.1868T= ENSP00000507751.1:p.Ile623=
ENST00000683220.1:c.1895T= ENSP00000507151.1:p.Ile632=
ENST00000683329.1:n.2668T=
ENST00000683346.1:c.*1740T= ENSP00000507458.1:n.*1740T=
ENST00000683459.1:n.2452T=
ENST00000683590.1:c.1865T= ENSP00000506820.1:p.Ile622=
ENST00000683623.1:c.1865T= ENSP00000507702.1:p.Ile622=
ENST00000683645.1:n.2416T=
ENST00000683694.1:n.616T=
ENST00000683796.1:c.*1737T= ENSP00000508221.1:n.*1737T=
ENST00000683802.1:n.4790T=
ENST00000683833.1:c.1856T= ENSP00000506852.1:p.Ile619=
ENST00000683934.1:c.1751T=
ENST00000683989.1:c.1865T= ENSP00000507510.1:p.Ile622=
ENST00000683994.1:c.1865T= ENSP00000507181.1:p.Ile622=
ENST00000684290.1:c.1865T= ENSP00000507243.1:p.Ile622=
ENST00000684306.1:c.*1778T= ENSP00000508384.1:n.*1778T=
ENST00000684341.1:n.1885T=
ENST00000684383.1:c.*1503T= ENSP00000506863.1:n.*1503T=
ENST00000684482.1:c.4334T=
ENST00000684619.1:c.*1737T= ENSP00000508088.1:n.*1737T=
ENST00000684743.1:n.2896T=
ENST00000260665.12:c.1865T= MANE Select ENSP00000260665.7:p.Ile622=
ENST00000260665.11:c.1865T= ENSP00000260665.7:p.Ile622=
NM_133259.3:c.1865T= NP_573566.2:p.Ile622=
XM_006711915.2:c.1787T= XP_006711978.1:p.Ile596=
XM_006711916.2:c.1865T= XP_006711979.1:p.Ile622=
XM_011532473.1:c.1865T= XP_011530775.1:p.Ile622=
XM_011532474.1:c.1865T= XP_011530776.1:p.Ile622=
XM_006711916.3:c.1865T= XP_006711979.1:p.Ile622=
XM_017003117.1:c.1787T= XP_016858606.1:p.Ile596=
XR_002958896.1:n.1907T=
NM_133259.4:c.1865T= MANE Select NP_573566.2:p.Ile622=