Canonical Allele Identifier: CA2658834446

Gene: LRPPRC

Linked Data

• ClinVar Variation Id: 2898145
• ClinVar RCV Id: RCV003726241
• gnomAD v4: 2-43899345-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43899346del , CM000664.2:g.43899346del	GRCh38
NC_000002.11:g.44126485del , CM000664.1:g.44126485del	GRCh37
NC_000002.10:g.43979989del	NCBI36
NG_008247.1:g.101660del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419884.6:c.141-12del
ENST00000472420.6:n.789-12del
ENST00000483489.2:n.141-12del
ENST00000681993.1:n.1262-12del
ENST00000682303.1:c.*3496-12del	ENSP00000508325.1:n.*3496-12del
ENST00000682308.1:c.3710-12del	ENSP00000507056.1:n.3710-12del
ENST00000682434.1:n.1261-12del
ENST00000682480.1:c.3728-12del	ENSP00000508344.1:n.3728-12del
ENST00000682546.1:c.3707-12del	ENSP00000508188.1:n.3707-12del
ENST00000682585.1:c.3710-12del	ENSP00000506885.1:n.3710-12del
ENST00000682595.1:n.4294-12del
ENST00000682607.1:c.2128-12del
ENST00000682612.1:c.562-12del
ENST00000682779.1:c.3701-12del	ENSP00000507947.1:n.3701-12del
ENST00000682845.1:n.2812-12del
ENST00000682885.1:c.3665-12del	ENSP00000508036.1:n.3665-12del
ENST00000682933.1:n.3784-12del
ENST00000683002.1:c.562-12del
ENST00000683072.1:n.4294-12del
ENST00000683080.1:n.1329-12del
ENST00000683125.1:c.3818-12del	ENSP00000507939.1:n.3818-12del
ENST00000683213.1:c.3713-12del	ENSP00000507751.1:n.3713-12del
ENST00000683220.1:c.3740-12del	ENSP00000507151.1:n.3740-12del
ENST00000683329.1:n.4513-12del
ENST00000683346.1:c.*3585-12del	ENSP00000507458.1:n.*3585-12del
ENST00000683409.1:n.2317-12del
ENST00000683459.1:n.4297-12del
ENST00000683528.1:c.638-12del
ENST00000683590.1:c.3458-12del	ENSP00000506820.1:n.3458-12del
ENST00000683623.1:c.3617-12del	ENSP00000507702.1:n.3617-12del
ENST00000683645.1:n.4261-12del
ENST00000683796.1:c.*3582-12del	ENSP00000508221.1:n.*3582-12del
ENST00000683802.1:n.6635-12del
ENST00000683833.1:c.3701-12del	ENSP00000506852.1:n.3701-12del
ENST00000683994.1:c.3710-12del	ENSP00000507181.1:n.3710-12del
ENST00000684290.1:c.*1246-12del	ENSP00000507243.1:n.*1246-12del
ENST00000684306.1:c.*3623-12del	ENSP00000508384.1:n.*3623-12del
ENST00000684341.1:n.3730-12del
ENST00000684383.1:c.*3348-12del	ENSP00000506863.1:n.*3348-12del
ENST00000684418.1:n.4891-12del
ENST00000684433.1:n.82del
ENST00000684454.1:n.3060-12del
ENST00000684619.1:c.*3582-12del	ENSP00000508088.1:n.*3582-12del
ENST00000684743.1:n.6455-12del
ENST00000260665.12:c.3710-12del MANE Select	ENSP00000260665.7:n.3710-12del
ENST00000260665.11:c.3710-12del	ENSP00000260665.7:n.3710-12del
ENST00000463456.5:n.2753-12del
ENST00000472420.5:n.107-12del
ENST00000483489.1:n.184-12del
NM_133259.3:c.3710-12del	NP_573566.2:n.3710-12del
XM_006711915.2:c.3632-12del	XP_006711978.1:n.3632-12del
XM_011532473.1:c.3710-12del	XP_011530775.1:n.3710-12del
XM_011532474.1:c.3710-12del	XP_011530776.1:n.3710-12del
XM_017003117.1:c.3632-12del	XP_016858606.1:n.3632-12del
XR_002958896.1:n.3752-12del
NM_133259.4:c.3710-12del MANE Select	NP_573566.2:n.3710-12del