Canonical Allele Identifier: CA2493977755

Gene: LRPPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43898927_43898928delinsTA , CM000664.2:g.43898927_43898928delinsTA	GRCh38
NC_000002.11:g.44126066_44126067delinsTA , CM000664.1:g.44126066_44126067delinsTA	GRCh37
NC_000002.10:g.43979570_43979571delinsTA	NCBI36
NG_008247.1:g.102078_102079delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419884.6:c.256+291_256+292delinsTA
ENST00000472420.6:n.904+291_904+292delinsTA
ENST00000483489.2:n.256+291_256+292delinsTA
ENST00000681993.1:n.1377+291_1377+292delinsTA
ENST00000682303.1:c.*3611+291_*3611+292delinsTA	ENSP00000508325.1:n.*3611+291_*3611+292delinsTA
ENST00000682308.1:c.3825+291_3825+292delinsTA	ENSP00000507056.1:n.3825+291_3825+292delinsTA
ENST00000682434.1:n.1376+291_1376+292delinsTA
ENST00000682480.1:c.3843+291_3843+292delinsTA	ENSP00000508344.1:n.3843+291_3843+292delinsTA
ENST00000682546.1:c.3822+291_3822+292delinsTA	ENSP00000508188.1:n.3822+291_3822+292delinsTA
ENST00000682585.1:c.3825+291_3825+292delinsTA	ENSP00000506885.1:n.3825+291_3825+292delinsTA
ENST00000682595.1:n.4409+291_4409+292delinsTA
ENST00000682607.1:c.2243+291_2243+292delinsTA
ENST00000682612.1:c.677+291_677+292delinsTA
ENST00000682779.1:c.3816+291_3816+292delinsTA	ENSP00000507947.1:n.3816+291_3816+292delinsTA
ENST00000682885.1:c.3780+291_3780+292delinsTA	ENSP00000508036.1:n.3780+291_3780+292delinsTA
ENST00000682933.1:n.3899+291_3899+292delinsTA
ENST00000683002.1:c.677+291_677+292delinsTA
ENST00000683072.1:n.4409+291_4409+292delinsTA
ENST00000683080.1:n.1444+291_1444+292delinsTA
ENST00000683125.1:c.3933+291_3933+292delinsTA	ENSP00000507939.1:n.3933+291_3933+292delinsTA
ENST00000683213.1:c.3828+291_3828+292delinsTA	ENSP00000507751.1:n.3828+291_3828+292delinsTA
ENST00000683220.1:c.3855+291_3855+292delinsTA	ENSP00000507151.1:n.3855+291_3855+292delinsTA
ENST00000683329.1:n.4628+291_4628+292delinsTA
ENST00000683346.1:c.*3700+291_*3700+292delinsTA	ENSP00000507458.1:n.*3700+291_*3700+292delinsTA
ENST00000683409.1:n.2432+291_2432+292delinsTA
ENST00000683459.1:n.4412+291_4412+292delinsTA
ENST00000683590.1:c.3573+291_3573+292delinsTA	ENSP00000506820.1:n.3573+291_3573+292delinsTA
ENST00000683623.1:c.3732+291_3732+292delinsTA	ENSP00000507702.1:n.3732+291_3732+292delinsTA
ENST00000683645.1:n.4667_4668delinsTA
ENST00000683796.1:c.*3697+291_*3697+292delinsTA	ENSP00000508221.1:n.*3697+291_*3697+292delinsTA
ENST00000683833.1:c.3816+291_3816+292delinsTA	ENSP00000506852.1:n.3816+291_3816+292delinsTA
ENST00000683994.1:c.3825+291_3825+292delinsTA	ENSP00000507181.1:n.3825+291_3825+292delinsTA
ENST00000684290.1:c.*1361+291_*1361+292delinsTA	ENSP00000507243.1:n.*1361+291_*1361+292delinsTA
ENST00000684306.1:c.*3738+291_*3738+292delinsTA	ENSP00000508384.1:n.*3738+291_*3738+292delinsTA
ENST00000684341.1:n.3845+291_3845+292delinsTA
ENST00000684383.1:c.*3463+291_*3463+292delinsTA	ENSP00000506863.1:n.*3463+291_*3463+292delinsTA
ENST00000684418.1:n.5006+291_5006+292delinsTA
ENST00000684433.1:n.209+291_209+292delinsTA
ENST00000684454.1:n.3466_3467delinsTA
ENST00000684619.1:c.*3697+291_*3697+292delinsTA	ENSP00000508088.1:n.*3697+291_*3697+292delinsTA
ENST00000684743.1:n.6570+291_6570+292delinsTA
ENST00000260665.12:c.3825+291_3825+292delinsTA MANE Select	ENSP00000260665.7:n.3825+291_3825+292delinsTA
ENST00000260665.11:c.3825+291_3825+292delinsTA	ENSP00000260665.7:n.3825+291_3825+292delinsTA
ENST00000419884.5:c.66+291_66+292delinsTA	ENSP00000414207.1:n.66+291_66+292delinsTA
ENST00000463456.5:n.2868+291_2868+292delinsTA
ENST00000472420.5:n.222+291_222+292delinsTA
ENST00000483489.1:n.299+291_299+292delinsTA
NM_133259.3:c.3825+291_3825+292delinsTA	NP_573566.2:n.3825+291_3825+292delinsTA
XM_006711915.2:c.3747+291_3747+292delinsTA	XP_006711978.1:n.3747+291_3747+292delinsTA
XM_011532473.1:c.3825+291_3825+292delinsTA	XP_011530775.1:n.3825+291_3825+292delinsTA
XM_011532474.1:c.3825+291_3825+292delinsTA	XP_011530776.1:n.3825+291_3825+292delinsTA
XM_017003117.1:c.3747+291_3747+292delinsTA	XP_016858606.1:n.3747+291_3747+292delinsTA
XR_002958896.1:n.3867+291_3867+292delinsTA
NM_133259.4:c.3825+291_3825+292delinsTA MANE Select	NP_573566.2:n.3825+291_3825+292delinsTA