Canonical Allele Identifier: CA2576954006

Gene: LRPPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43894478_43894479del , CM000664.2:g.43894478_43894479del	GRCh38
NC_000002.11:g.44121617_44121618del , CM000664.1:g.44121617_44121618del	GRCh37
NC_000002.10:g.43975121_43975122del	NCBI36
NG_008247.1:g.106527_106528del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419884.6:c.615+66_615+67del
ENST00000681993.1:n.1537+66_1537+67del
ENST00000682154.1:n.1419+66_1419+67del
ENST00000682303.1:c.*3696+66_*3696+67del	ENSP00000508325.1:n.*3696+66_*3696+67del
ENST00000682308.1:c.3910+66_3910+67del	ENSP00000507056.1:n.3910+66_3910+67del
ENST00000682434.1:n.3540+66_3540+67del
ENST00000682480.1:c.4003+66_4003+67del	ENSP00000508344.1:n.4003+66_4003+67del
ENST00000682546.1:c.3982+66_3982+67del	ENSP00000508188.1:n.3982+66_3982+67del
ENST00000682585.1:c.*113+66_*113+67del	ENSP00000506885.1:n.*113+66_*113+67del
ENST00000682607.1:c.2728+66_2728+67del
ENST00000682612.1:c.752+2155_752+2156del
ENST00000682696.1:c.85+66_85+67del	ENSP00000508411.1:n.85+66_85+67del
ENST00000682779.1:c.3976+66_3976+67del	ENSP00000507947.1:n.3976+66_3976+67del
ENST00000682885.1:c.3940+66_3940+67del	ENSP00000508036.1:n.3940+66_3940+67del
ENST00000682933.1:n.4185+66_4185+67del
ENST00000683002.1:c.837+66_837+67del
ENST00000683072.1:n.4569+66_4569+67del
ENST00000683080.1:n.1604+66_1604+67del
ENST00000683096.1:n.2426+66_2426+67del
ENST00000683125.1:c.4093+66_4093+67del	ENSP00000507939.1:n.4093+66_4093+67del
ENST00000683213.1:c.3988+66_3988+67del	ENSP00000507751.1:n.3988+66_3988+67del
ENST00000683220.1:c.4015+66_4015+67del	ENSP00000507151.1:n.4015+66_4015+67del
ENST00000683329.1:n.4788+66_4788+67del
ENST00000683346.1:c.*3860+66_*3860+67del	ENSP00000507458.1:n.*3860+66_*3860+67del
ENST00000683409.1:n.2517+66_2517+67del
ENST00000683459.1:n.4572+66_4572+67del
ENST00000683590.1:c.3658+66_3658+67del	ENSP00000506820.1:n.3658+66_3658+67del
ENST00000683623.1:c.3892+66_3892+67del	ENSP00000507702.1:n.3892+66_3892+67del
ENST00000683796.1:c.*3782+66_*3782+67del	ENSP00000508221.1:n.*3782+66_*3782+67del
ENST00000683833.1:c.3901+66_3901+67del	ENSP00000506852.1:n.3901+66_3901+67del
ENST00000683994.1:c.*98+66_*98+67del	ENSP00000507181.1:n.*98+66_*98+67del
ENST00000684290.1:c.*1446+66_*1446+67del	ENSP00000507243.1:n.*1446+66_*1446+67del
ENST00000684306.1:c.*3898+66_*3898+67del	ENSP00000508384.1:n.*3898+66_*3898+67del
ENST00000684383.1:c.*3623+66_*3623+67del	ENSP00000506863.1:n.*3623+66_*3623+67del
ENST00000684418.1:n.5166+66_5166+67del
ENST00000684433.1:n.369+66_369+67del
ENST00000684454.1:n.7849+66_7849+67del
ENST00000684619.1:c.*3857+66_*3857+67del	ENSP00000508088.1:n.*3857+66_*3857+67del
ENST00000684743.1:n.6730+66_6730+67del
ENST00000260665.12:c.3985+66_3985+67del MANE Select	ENSP00000260665.7:n.3985+66_3985+67del
ENST00000260665.11:c.3985+66_3985+67del	ENSP00000260665.7:n.3985+66_3985+67del
ENST00000419884.5:c.226+66_226+67del	ENSP00000414207.1:n.226+66_226+67del
ENST00000463456.5:n.3028+66_3028+67del
NM_133259.3:c.3985+66_3985+67del	NP_573566.2:n.3985+66_3985+67del
XM_006711915.2:c.3907+66_3907+67del	XP_006711978.1:n.3907+66_3907+67del
XM_011532473.1:c.3910+66_3910+67del	XP_011530775.1:n.3910+66_3910+67del
XM_011532474.1:c.3985+66_3985+67del	XP_011530776.1:n.3985+66_3985+67del
XM_017003117.1:c.3832+66_3832+67del	XP_016858606.1:n.3832+66_3832+67del
XR_002958896.1:n.4027+66_4027+67del
NM_133259.4:c.3985+66_3985+67del MANE Select	NP_573566.2:n.3985+66_3985+67del