Canonical Allele Identifier: CA2494004467
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43948462G= , CM000664.2:g.43948462G= GRCh38
NC_000002.11:g.44175601G= , CM000664.1:g.44175601G= GRCh37
NC_000002.10:g.44029105G= NCBI36
NG_008247.1:g.52544C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409659.6:c.1792C= ENSP00000386562.2:p.Gln598=
ENST00000447246.2:c.1792C= ENSP00000403637.2:p.Gln598=
ENST00000467058.2:n.521C=
ENST00000681959.1:n.1406C=
ENST00000681961.1:n.1812C=
ENST00000682104.1:c.1666C= ENSP00000507716.1:p.Gln556=
ENST00000682303.1:c.*1664C= ENSP00000508325.1:n.*1664C=
ENST00000682308.1:c.1792C= ENSP00000507056.1:p.Gln598=
ENST00000682480.1:c.1792C= ENSP00000508344.1:p.Gln598=
ENST00000682546.1:c.1789C= ENSP00000508188.1:p.Gln597=
ENST00000682585.1:c.1792C= ENSP00000506885.1:p.Gln598=
ENST00000682595.1:n.2374C=
ENST00000682607.1:c.210C=
ENST00000682779.1:c.1783C= ENSP00000507947.1:p.Gln595=
ENST00000682885.1:c.1792C= ENSP00000508036.1:p.Gln598=
ENST00000682933.1:n.1866C=
ENST00000683072.1:n.2374C=
ENST00000683082.1:n.1810C=
ENST00000683125.1:c.1792C= ENSP00000507939.1:p.Gln598=
ENST00000683213.1:c.1795C= ENSP00000507751.1:p.Gln599=
ENST00000683220.1:c.1822C= ENSP00000507151.1:p.Gln608=
ENST00000683329.1:n.2595C=
ENST00000683346.1:c.*1667C= ENSP00000507458.1:n.*1667C=
ENST00000683459.1:n.2379C=
ENST00000683590.1:c.1792C= ENSP00000506820.1:p.Gln598=
ENST00000683623.1:c.1792C= ENSP00000507702.1:p.Gln598=
ENST00000683645.1:n.2312C=
ENST00000683694.1:n.543C=
ENST00000683796.1:c.*1664C= ENSP00000508221.1:n.*1664C=
ENST00000683802.1:n.4717C=
ENST00000683833.1:c.1783C= ENSP00000506852.1:p.Gln595=
ENST00000683934.1:c.1678C=
ENST00000683989.1:c.1792C= ENSP00000507510.1:p.Gln598=
ENST00000683994.1:c.1792C= ENSP00000507181.1:p.Gln598=
ENST00000684290.1:c.1792C= ENSP00000507243.1:p.Gln598=
ENST00000684306.1:c.*1705C= ENSP00000508384.1:n.*1705C=
ENST00000684341.1:n.1812C=
ENST00000684383.1:c.*1430C= ENSP00000506863.1:n.*1430C=
ENST00000684482.1:c.4261C=
ENST00000684619.1:c.*1664C= ENSP00000508088.1:n.*1664C=
ENST00000684743.1:n.2823C=
ENST00000260665.12:c.1792C= MANE Select ENSP00000260665.7:p.Gln598=
ENST00000260665.11:c.1792C= ENSP00000260665.7:p.Gln598=
ENST00000467058.1:n.521C=
NM_133259.3:c.1792C= NP_573566.2:p.Gln598=
XM_006711915.2:c.1714C= XP_006711978.1:p.Gln572=
XM_006711916.2:c.1792C= XP_006711979.1:p.Gln598=
XM_011532473.1:c.1792C= XP_011530775.1:p.Gln598=
XM_011532474.1:c.1792C= XP_011530776.1:p.Gln598=
XM_006711916.3:c.1792C= XP_006711979.1:p.Gln598=
XM_017003117.1:c.1714C= XP_016858606.1:p.Gln572=
XR_002958896.1:n.1834C=
NM_133259.4:c.1792C= MANE Select NP_573566.2:p.Gln598=