Canonical Allele Identifier: CA2493977814

Gene: LRPPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43899021_43899022delinsTG , CM000664.2:g.43899021_43899022delinsTG	GRCh38
NC_000002.11:g.44126160_44126161delinsTG , CM000664.1:g.44126160_44126161delinsTG	GRCh37
NC_000002.10:g.43979664_43979665delinsTG	NCBI36
NG_008247.1:g.101984_101985delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419884.6:c.256+197_256+198delinsCA
ENST00000472420.6:n.904+197_904+198delinsCA
ENST00000483489.2:n.256+197_256+198delinsCA
ENST00000681993.1:n.1377+197_1377+198delinsCA
ENST00000682303.1:c.*3611+197_*3611+198delinsCA	ENSP00000508325.1:n.*3611+197_*3611+198delinsCA
ENST00000682308.1:c.3825+197_3825+198delinsCA	ENSP00000507056.1:n.3825+197_3825+198delinsCA
ENST00000682434.1:n.1376+197_1376+198delinsCA
ENST00000682480.1:c.3843+197_3843+198delinsCA	ENSP00000508344.1:n.3843+197_3843+198delinsCA
ENST00000682546.1:c.3822+197_3822+198delinsCA	ENSP00000508188.1:n.3822+197_3822+198delinsCA
ENST00000682585.1:c.3825+197_3825+198delinsCA	ENSP00000506885.1:n.3825+197_3825+198delinsCA
ENST00000682595.1:n.4409+197_4409+198delinsCA
ENST00000682607.1:c.2243+197_2243+198delinsCA
ENST00000682612.1:c.677+197_677+198delinsCA
ENST00000682779.1:c.3816+197_3816+198delinsCA	ENSP00000507947.1:n.3816+197_3816+198delinsCA
ENST00000682885.1:c.3780+197_3780+198delinsCA	ENSP00000508036.1:n.3780+197_3780+198delinsCA
ENST00000682933.1:n.3899+197_3899+198delinsCA
ENST00000683002.1:c.677+197_677+198delinsCA
ENST00000683072.1:n.4409+197_4409+198delinsCA
ENST00000683080.1:n.1444+197_1444+198delinsCA
ENST00000683125.1:c.3933+197_3933+198delinsCA	ENSP00000507939.1:n.3933+197_3933+198delinsCA
ENST00000683213.1:c.3828+197_3828+198delinsCA	ENSP00000507751.1:n.3828+197_3828+198delinsCA
ENST00000683220.1:c.3855+197_3855+198delinsCA	ENSP00000507151.1:n.3855+197_3855+198delinsCA
ENST00000683329.1:n.4628+197_4628+198delinsCA
ENST00000683346.1:c.*3700+197_*3700+198delinsCA	ENSP00000507458.1:n.*3700+197_*3700+198delinsCA
ENST00000683409.1:n.2432+197_2432+198delinsCA
ENST00000683459.1:n.4412+197_4412+198delinsCA
ENST00000683590.1:c.3573+197_3573+198delinsCA	ENSP00000506820.1:n.3573+197_3573+198delinsCA
ENST00000683623.1:c.3732+197_3732+198delinsCA	ENSP00000507702.1:n.3732+197_3732+198delinsCA
ENST00000683645.1:n.4573_4574delinsCA
ENST00000683796.1:c.*3697+197_*3697+198delinsCA	ENSP00000508221.1:n.*3697+197_*3697+198delinsCA
ENST00000683833.1:c.3816+197_3816+198delinsCA	ENSP00000506852.1:n.3816+197_3816+198delinsCA
ENST00000683994.1:c.3825+197_3825+198delinsCA	ENSP00000507181.1:n.3825+197_3825+198delinsCA
ENST00000684290.1:c.*1361+197_*1361+198delinsCA	ENSP00000507243.1:n.*1361+197_*1361+198delinsCA
ENST00000684306.1:c.*3738+197_*3738+198delinsCA	ENSP00000508384.1:n.*3738+197_*3738+198delinsCA
ENST00000684341.1:n.3845+197_3845+198delinsCA
ENST00000684383.1:c.*3463+197_*3463+198delinsCA	ENSP00000506863.1:n.*3463+197_*3463+198delinsCA
ENST00000684418.1:n.5006+197_5006+198delinsCA
ENST00000684433.1:n.209+197_209+198delinsCA
ENST00000684454.1:n.3372_3373delinsCA
ENST00000684619.1:c.*3697+197_*3697+198delinsCA	ENSP00000508088.1:n.*3697+197_*3697+198delinsCA
ENST00000684743.1:n.6570+197_6570+198delinsCA
ENST00000260665.12:c.3825+197_3825+198delinsCA MANE Select	ENSP00000260665.7:n.3825+197_3825+198delinsCA
ENST00000260665.11:c.3825+197_3825+198delinsCA	ENSP00000260665.7:n.3825+197_3825+198delinsCA
ENST00000419884.5:c.66+197_66+198delinsCA	ENSP00000414207.1:n.66+197_66+198delinsCA
ENST00000463456.5:n.2868+197_2868+198delinsCA
ENST00000472420.5:n.222+197_222+198delinsCA
ENST00000483489.1:n.299+197_299+198delinsCA
NM_133259.3:c.3825+197_3825+198delinsCA	NP_573566.2:n.3825+197_3825+198delinsCA
XM_006711915.2:c.3747+197_3747+198delinsCA	XP_006711978.1:n.3747+197_3747+198delinsCA
XM_011532473.1:c.3825+197_3825+198delinsCA	XP_011530775.1:n.3825+197_3825+198delinsCA
XM_011532474.1:c.3825+197_3825+198delinsCA	XP_011530776.1:n.3825+197_3825+198delinsCA
XM_017003117.1:c.3747+197_3747+198delinsCA	XP_016858606.1:n.3747+197_3747+198delinsCA
XR_002958896.1:n.3867+197_3867+198delinsCA
NM_133259.4:c.3825+197_3825+198delinsCA MANE Select	NP_573566.2:n.3825+197_3825+198delinsCA