Canonical Allele Identifier: CA2658833929

Gene: LRPPRC

Linked Data

• gnomAD v4: 2-43894525-TCAAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43894526_43894529del , CM000664.2:g.43894526_43894529del	GRCh38
NC_000002.11:g.44121665_44121668del , CM000664.1:g.44121665_44121668del	GRCh37
NC_000002.10:g.43975169_43975172del	NCBI36
NG_008247.1:g.106477_106480del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419884.6:c.615+16_615+19del
ENST00000681993.1:n.1537+16_1537+19del
ENST00000682154.1:n.1419+16_1419+19del
ENST00000682303.1:c.*3696+16_*3696+19del	ENSP00000508325.1:n.*3696+16_*3696+19del
ENST00000682308.1:c.3910+16_3910+19del	ENSP00000507056.1:n.3910+16_3910+19del
ENST00000682434.1:n.3540+16_3540+19del
ENST00000682480.1:c.4003+16_4003+19del	ENSP00000508344.1:n.4003+16_4003+19del
ENST00000682546.1:c.3982+16_3982+19del	ENSP00000508188.1:n.3982+16_3982+19del
ENST00000682585.1:c.*113+16_*113+19del	ENSP00000506885.1:n.*113+16_*113+19del
ENST00000682607.1:c.2728+16_2728+19del
ENST00000682612.1:c.752+2105_752+2108del
ENST00000682696.1:c.85+16_85+19del	ENSP00000508411.1:n.85+16_85+19del
ENST00000682779.1:c.3976+16_3976+19del	ENSP00000507947.1:n.3976+16_3976+19del
ENST00000682885.1:c.3940+16_3940+19del	ENSP00000508036.1:n.3940+16_3940+19del
ENST00000682933.1:n.4185+16_4185+19del
ENST00000683002.1:c.837+16_837+19del
ENST00000683072.1:n.4569+16_4569+19del
ENST00000683080.1:n.1604+16_1604+19del
ENST00000683096.1:n.2426+16_2426+19del
ENST00000683125.1:c.4093+16_4093+19del	ENSP00000507939.1:n.4093+16_4093+19del
ENST00000683213.1:c.3988+16_3988+19del	ENSP00000507751.1:n.3988+16_3988+19del
ENST00000683220.1:c.4015+16_4015+19del	ENSP00000507151.1:n.4015+16_4015+19del
ENST00000683329.1:n.4788+16_4788+19del
ENST00000683346.1:c.*3860+16_*3860+19del	ENSP00000507458.1:n.*3860+16_*3860+19del
ENST00000683409.1:n.2517+16_2517+19del
ENST00000683459.1:n.4572+16_4572+19del
ENST00000683590.1:c.3658+16_3658+19del	ENSP00000506820.1:n.3658+16_3658+19del
ENST00000683623.1:c.3892+16_3892+19del	ENSP00000507702.1:n.3892+16_3892+19del
ENST00000683796.1:c.*3782+16_*3782+19del	ENSP00000508221.1:n.*3782+16_*3782+19del
ENST00000683833.1:c.3901+16_3901+19del	ENSP00000506852.1:n.3901+16_3901+19del
ENST00000683994.1:c.*98+16_*98+19del	ENSP00000507181.1:n.*98+16_*98+19del
ENST00000684290.1:c.*1446+16_*1446+19del	ENSP00000507243.1:n.*1446+16_*1446+19del
ENST00000684306.1:c.*3898+16_*3898+19del	ENSP00000508384.1:n.*3898+16_*3898+19del
ENST00000684383.1:c.*3623+16_*3623+19del	ENSP00000506863.1:n.*3623+16_*3623+19del
ENST00000684418.1:n.5166+16_5166+19del
ENST00000684433.1:n.369+16_369+19del
ENST00000684454.1:n.7849+16_7849+19del
ENST00000684619.1:c.*3857+16_*3857+19del	ENSP00000508088.1:n.*3857+16_*3857+19del
ENST00000684743.1:n.6730+16_6730+19del
ENST00000260665.12:c.3985+16_3985+19del MANE Select	ENSP00000260665.7:n.3985+16_3985+19del
ENST00000260665.11:c.3985+16_3985+19del	ENSP00000260665.7:n.3985+16_3985+19del
ENST00000419884.5:c.226+16_226+19del	ENSP00000414207.1:n.226+16_226+19del
ENST00000463456.5:n.3028+16_3028+19del
NM_133259.3:c.3985+16_3985+19del	NP_573566.2:n.3985+16_3985+19del
XM_006711915.2:c.3907+16_3907+19del	XP_006711978.1:n.3907+16_3907+19del
XM_011532473.1:c.3910+16_3910+19del	XP_011530775.1:n.3910+16_3910+19del
XM_011532474.1:c.3985+16_3985+19del	XP_011530776.1:n.3985+16_3985+19del
XM_017003117.1:c.3832+16_3832+19del	XP_016858606.1:n.3832+16_3832+19del
XR_002958896.1:n.4027+16_4027+19del
NM_133259.4:c.3985+16_3985+19del MANE Select	NP_573566.2:n.3985+16_3985+19del