Canonical Allele Identifier: CA2494009354

Gene: LRPPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43957281_43957284delinsACTG , CM000664.2:g.43957281_43957284delinsACTG	GRCh38
NC_000002.11:g.44184420_44184423delinsACTG , CM000664.1:g.44184420_44184423delinsACTG	GRCh37
NC_000002.10:g.44037924_44037927delinsACTG	NCBI36
NG_008247.1:g.43722_43725delinsCAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409659.6:c.1649+101_1649+104delinsCAGT	ENSP00000386562.2:n.1649+101_1649+104delinsCAGT
ENST00000447246.2:c.1649+101_1649+104delinsCAGT	ENSP00000403637.2:n.1649+101_1649+104delinsCAGT
ENST00000467058.2:n.378+101_378+104delinsCAGT
ENST00000681959.1:n.1263+101_1263+104delinsCAGT
ENST00000681961.1:n.1669+101_1669+104delinsCAGT
ENST00000682104.1:c.1523+101_1523+104delinsCAGT	ENSP00000507716.1:n.1523+101_1523+104delinsCAGT
ENST00000682303.1:c.*1521+101_*1521+104delinsCAGT	ENSP00000508325.1:n.*1521+101_*1521+104delinsCAGT
ENST00000682308.1:c.1649+101_1649+104delinsCAGT	ENSP00000507056.1:n.1649+101_1649+104delinsCAGT
ENST00000682480.1:c.1649+101_1649+104delinsCAGT	ENSP00000508344.1:n.1649+101_1649+104delinsCAGT
ENST00000682546.1:c.1649+101_1649+104delinsCAGT	ENSP00000508188.1:n.1649+101_1649+104delinsCAGT
ENST00000682585.1:c.1649+101_1649+104delinsCAGT	ENSP00000506885.1:n.1649+101_1649+104delinsCAGT
ENST00000682595.1:n.2231+101_2231+104delinsCAGT
ENST00000682607.1:c.67+101_67+104delinsCAGT
ENST00000682779.1:c.1640+101_1640+104delinsCAGT	ENSP00000507947.1:n.1640+101_1640+104delinsCAGT
ENST00000682885.1:c.1649+101_1649+104delinsCAGT	ENSP00000508036.1:n.1649+101_1649+104delinsCAGT
ENST00000682933.1:n.1723+101_1723+104delinsCAGT
ENST00000683072.1:n.2231+101_2231+104delinsCAGT
ENST00000683082.1:n.1667+101_1667+104delinsCAGT
ENST00000683125.1:c.1649+101_1649+104delinsCAGT	ENSP00000507939.1:n.1649+101_1649+104delinsCAGT
ENST00000683213.1:c.1652+101_1652+104delinsCAGT	ENSP00000507751.1:n.1652+101_1652+104delinsCAGT
ENST00000683220.1:c.1649+101_1649+104delinsCAGT	ENSP00000507151.1:n.1649+101_1649+104delinsCAGT
ENST00000683329.1:n.2452+101_2452+104delinsCAGT
ENST00000683346.1:c.*1524+101_*1524+104delinsCAGT	ENSP00000507458.1:n.*1524+101_*1524+104delinsCAGT
ENST00000683459.1:n.2236+101_2236+104delinsCAGT
ENST00000683590.1:c.1649+101_1649+104delinsCAGT	ENSP00000506820.1:n.1649+101_1649+104delinsCAGT
ENST00000683623.1:c.1649+101_1649+104delinsCAGT	ENSP00000507702.1:n.1649+101_1649+104delinsCAGT
ENST00000683645.1:n.2169+101_2169+104delinsCAGT
ENST00000683694.1:n.400+101_400+104delinsCAGT
ENST00000683796.1:c.*1521+101_*1521+104delinsCAGT	ENSP00000508221.1:n.*1521+101_*1521+104delinsCAGT
ENST00000683802.1:n.4574+101_4574+104delinsCAGT
ENST00000683833.1:c.1640+101_1640+104delinsCAGT	ENSP00000506852.1:n.1640+101_1640+104delinsCAGT
ENST00000683934.1:c.1535+101_1535+104delinsCAGT
ENST00000683989.1:c.1649+101_1649+104delinsCAGT	ENSP00000507510.1:n.1649+101_1649+104delinsCAGT
ENST00000683994.1:c.1649+101_1649+104delinsCAGT	ENSP00000507181.1:n.1649+101_1649+104delinsCAGT
ENST00000684290.1:c.1649+101_1649+104delinsCAGT	ENSP00000507243.1:n.1649+101_1649+104delinsCAGT
ENST00000684306.1:c.*1562+101_*1562+104delinsCAGT	ENSP00000508384.1:n.*1562+101_*1562+104delinsCAGT
ENST00000684341.1:n.1669+101_1669+104delinsCAGT
ENST00000684383.1:c.*1287+101_*1287+104delinsCAGT	ENSP00000506863.1:n.*1287+101_*1287+104delinsCAGT
ENST00000684482.1:c.4118+101_4118+104delinsCAGT
ENST00000684619.1:c.*1521+101_*1521+104delinsCAGT	ENSP00000508088.1:n.*1521+101_*1521+104delinsCAGT
ENST00000684743.1:n.2680+101_2680+104delinsCAGT
ENST00000260665.12:c.1649+101_1649+104delinsCAGT MANE Select	ENSP00000260665.7:n.1649+101_1649+104delinsCAGT
ENST00000260665.11:c.1649+101_1649+104delinsCAGT	ENSP00000260665.7:n.1649+101_1649+104delinsCAGT
ENST00000467058.1:n.378+101_378+104delinsCAGT
NM_133259.3:c.1649+101_1649+104delinsCAGT	NP_573566.2:n.1649+101_1649+104delinsCAGT
XM_006711915.2:c.1571+101_1571+104delinsCAGT	XP_006711978.1:n.1571+101_1571+104delinsCAGT
XM_006711916.2:c.1649+101_1649+104delinsCAGT	XP_006711979.1:n.1649+101_1649+104delinsCAGT
XM_011532473.1:c.1649+101_1649+104delinsCAGT	XP_011530775.1:n.1649+101_1649+104delinsCAGT
XM_011532474.1:c.1649+101_1649+104delinsCAGT	XP_011530776.1:n.1649+101_1649+104delinsCAGT
XM_006711916.3:c.1649+101_1649+104delinsCAGT	XP_006711979.1:n.1649+101_1649+104delinsCAGT
XM_017003117.1:c.1571+101_1571+104delinsCAGT	XP_016858606.1:n.1571+101_1571+104delinsCAGT
XR_002958896.1:n.1691+101_1691+104delinsCAGT
NM_133259.4:c.1649+101_1649+104delinsCAGT MANE Select	NP_573566.2:n.1649+101_1649+104delinsCAGT