Canonical Allele Identifier: CA2493975239

Gene: LRPPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43894526_43894531delinsCAAATT , CM000664.2:g.43894526_43894531delinsCAAATT	GRCh38
NC_000002.11:g.44121665_44121670delinsCAAATT , CM000664.1:g.44121665_44121670delinsCAAATT	GRCh37
NC_000002.10:g.43975169_43975174delinsCAAATT	NCBI36
NG_008247.1:g.106475_106480delinsAATTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419884.6:c.615+14_615+19delinsAATTTG
ENST00000681993.1:n.1537+14_1537+19delinsAATTTG
ENST00000682154.1:n.1419+14_1419+19delinsAATTTG
ENST00000682303.1:c.*3696+14_*3696+19delinsAATTTG	ENSP00000508325.1:n.*3696+14_*3696+19delinsAATTTG
ENST00000682308.1:c.3910+14_3910+19delinsAATTTG	ENSP00000507056.1:n.3910+14_3910+19delinsAATTTG
ENST00000682434.1:n.3540+14_3540+19delinsAATTTG
ENST00000682480.1:c.4003+14_4003+19delinsAATTTG	ENSP00000508344.1:n.4003+14_4003+19delinsAATTTG
ENST00000682546.1:c.3982+14_3982+19delinsAATTTG	ENSP00000508188.1:n.3982+14_3982+19delinsAATTTG
ENST00000682585.1:c.*113+14_*113+19delinsAATTTG	ENSP00000506885.1:n.*113+14_*113+19delinsAATTTG
ENST00000682607.1:c.2728+14_2728+19delinsAATTTG
ENST00000682612.1:c.752+2103_752+2108delinsAATTTG
ENST00000682696.1:c.85+14_85+19delinsAATTTG	ENSP00000508411.1:n.85+14_85+19delinsAATTTG
ENST00000682779.1:c.3976+14_3976+19delinsAATTTG	ENSP00000507947.1:n.3976+14_3976+19delinsAATTTG
ENST00000682885.1:c.3940+14_3940+19delinsAATTTG	ENSP00000508036.1:n.3940+14_3940+19delinsAATTTG
ENST00000682933.1:n.4185+14_4185+19delinsAATTTG
ENST00000683002.1:c.837+14_837+19delinsAATTTG
ENST00000683072.1:n.4569+14_4569+19delinsAATTTG
ENST00000683080.1:n.1604+14_1604+19delinsAATTTG
ENST00000683096.1:n.2426+14_2426+19delinsAATTTG
ENST00000683125.1:c.4093+14_4093+19delinsAATTTG	ENSP00000507939.1:n.4093+14_4093+19delinsAATTTG
ENST00000683213.1:c.3988+14_3988+19delinsAATTTG	ENSP00000507751.1:n.3988+14_3988+19delinsAATTTG
ENST00000683220.1:c.4015+14_4015+19delinsAATTTG	ENSP00000507151.1:n.4015+14_4015+19delinsAATTTG
ENST00000683329.1:n.4788+14_4788+19delinsAATTTG
ENST00000683346.1:c.*3860+14_*3860+19delinsAATTTG	ENSP00000507458.1:n.*3860+14_*3860+19delinsAATTTG
ENST00000683409.1:n.2517+14_2517+19delinsAATTTG
ENST00000683459.1:n.4572+14_4572+19delinsAATTTG
ENST00000683590.1:c.3658+14_3658+19delinsAATTTG	ENSP00000506820.1:n.3658+14_3658+19delinsAATTTG
ENST00000683623.1:c.3892+14_3892+19delinsAATTTG	ENSP00000507702.1:n.3892+14_3892+19delinsAATTTG
ENST00000683796.1:c.*3782+14_*3782+19delinsAATTTG	ENSP00000508221.1:n.*3782+14_*3782+19delinsAATTTG
ENST00000683833.1:c.3901+14_3901+19delinsAATTTG	ENSP00000506852.1:n.3901+14_3901+19delinsAATTTG
ENST00000683994.1:c.*98+14_*98+19delinsAATTTG	ENSP00000507181.1:n.*98+14_*98+19delinsAATTTG
ENST00000684290.1:c.*1446+14_*1446+19delinsAATTTG	ENSP00000507243.1:n.*1446+14_*1446+19delinsAATTTG
ENST00000684306.1:c.*3898+14_*3898+19delinsAATTTG	ENSP00000508384.1:n.*3898+14_*3898+19delinsAATTTG
ENST00000684383.1:c.*3623+14_*3623+19delinsAATTTG	ENSP00000506863.1:n.*3623+14_*3623+19delinsAATTTG
ENST00000684418.1:n.5166+14_5166+19delinsAATTTG
ENST00000684433.1:n.369+14_369+19delinsAATTTG
ENST00000684454.1:n.7849+14_7849+19delinsAATTTG
ENST00000684619.1:c.*3857+14_*3857+19delinsAATTTG	ENSP00000508088.1:n.*3857+14_*3857+19delinsAATTTG
ENST00000684743.1:n.6730+14_6730+19delinsAATTTG
ENST00000260665.12:c.3985+14_3985+19delinsAATTTG MANE Select	ENSP00000260665.7:n.3985+14_3985+19delinsAATTTG
ENST00000260665.11:c.3985+14_3985+19delinsAATTTG	ENSP00000260665.7:n.3985+14_3985+19delinsAATTTG
ENST00000419884.5:c.226+14_226+19delinsAATTTG	ENSP00000414207.1:n.226+14_226+19delinsAATTTG
ENST00000463456.5:n.3028+14_3028+19delinsAATTTG
NM_133259.3:c.3985+14_3985+19delinsAATTTG	NP_573566.2:n.3985+14_3985+19delinsAATTTG
XM_006711915.2:c.3907+14_3907+19delinsAATTTG	XP_006711978.1:n.3907+14_3907+19delinsAATTTG
XM_011532473.1:c.3910+14_3910+19delinsAATTTG	XP_011530775.1:n.3910+14_3910+19delinsAATTTG
XM_011532474.1:c.3985+14_3985+19delinsAATTTG	XP_011530776.1:n.3985+14_3985+19delinsAATTTG
XM_017003117.1:c.3832+14_3832+19delinsAATTTG	XP_016858606.1:n.3832+14_3832+19delinsAATTTG
XR_002958896.1:n.4027+14_4027+19delinsAATTTG
NM_133259.4:c.3985+14_3985+19delinsAATTTG MANE Select	NP_573566.2:n.3985+14_3985+19delinsAATTTG