Canonical Allele Identifier: CA769099507

Gene: LRPPRC

Linked Data

• dbSNP Id: rs1481023297
• gnomAD v4: 2-43899077-G-GT
• MyVariant Identifiers: chr2:g.44126216_44126217insT (hg19) ; chr2:g.43899077_43899078insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43899078dup , CM000664.2:g.43899078dup	GRCh38
NC_000002.11:g.44126217dup , CM000664.1:g.44126217dup	GRCh37
NC_000002.10:g.43979721dup	NCBI36
NG_008247.1:g.101928dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419884.6:c.256+141dup
ENST00000472420.6:n.904+141dup
ENST00000483489.2:n.256+141dup
ENST00000681993.1:n.1377+141dup
ENST00000682303.1:c.*3611+141dup	ENSP00000508325.1:n.*3611+141dup
ENST00000682308.1:c.3825+141dup	ENSP00000507056.1:n.3825+141dup
ENST00000682434.1:n.1376+141dup
ENST00000682480.1:c.3843+141dup	ENSP00000508344.1:n.3843+141dup
ENST00000682546.1:c.3822+141dup	ENSP00000508188.1:n.3822+141dup
ENST00000682585.1:c.3825+141dup	ENSP00000506885.1:n.3825+141dup
ENST00000682595.1:n.4409+141dup
ENST00000682607.1:c.2243+141dup
ENST00000682612.1:c.677+141dup
ENST00000682779.1:c.3816+141dup	ENSP00000507947.1:n.3816+141dup
ENST00000682885.1:c.3780+141dup	ENSP00000508036.1:n.3780+141dup
ENST00000682933.1:n.3899+141dup
ENST00000683002.1:c.677+141dup
ENST00000683072.1:n.4409+141dup
ENST00000683080.1:n.1444+141dup
ENST00000683125.1:c.3933+141dup	ENSP00000507939.1:n.3933+141dup
ENST00000683213.1:c.3828+141dup	ENSP00000507751.1:n.3828+141dup
ENST00000683220.1:c.3855+141dup	ENSP00000507151.1:n.3855+141dup
ENST00000683329.1:n.4628+141dup
ENST00000683346.1:c.*3700+141dup	ENSP00000507458.1:n.*3700+141dup
ENST00000683409.1:n.2432+141dup
ENST00000683459.1:n.4412+141dup
ENST00000683590.1:c.3573+141dup	ENSP00000506820.1:n.3573+141dup
ENST00000683623.1:c.3732+141dup	ENSP00000507702.1:n.3732+141dup
ENST00000683645.1:n.4517dup
ENST00000683796.1:c.*3697+141dup	ENSP00000508221.1:n.*3697+141dup
ENST00000683833.1:c.3816+141dup	ENSP00000506852.1:n.3816+141dup
ENST00000683994.1:c.3825+141dup	ENSP00000507181.1:n.3825+141dup
ENST00000684290.1:c.*1361+141dup	ENSP00000507243.1:n.*1361+141dup
ENST00000684306.1:c.*3738+141dup	ENSP00000508384.1:n.*3738+141dup
ENST00000684341.1:n.3845+141dup
ENST00000684383.1:c.*3463+141dup	ENSP00000506863.1:n.*3463+141dup
ENST00000684418.1:n.5006+141dup
ENST00000684433.1:n.209+141dup
ENST00000684454.1:n.3316dup
ENST00000684619.1:c.*3697+141dup	ENSP00000508088.1:n.*3697+141dup
ENST00000684743.1:n.6570+141dup
ENST00000260665.12:c.3825+141dup MANE Select	ENSP00000260665.7:n.3825+141dup
ENST00000260665.11:c.3825+141dup	ENSP00000260665.7:n.3825+141dup
ENST00000419884.5:c.66+141dup	ENSP00000414207.1:n.66+141dup
ENST00000463456.5:n.2868+141dup
ENST00000472420.5:n.222+141dup
ENST00000483489.1:n.299+141dup
NM_133259.3:c.3825+141dup	NP_573566.2:n.3825+141dup
XM_006711915.2:c.3747+141dup	XP_006711978.1:n.3747+141dup
XM_011532473.1:c.3825+141dup	XP_011530775.1:n.3825+141dup
XM_011532474.1:c.3825+141dup	XP_011530776.1:n.3825+141dup
XM_017003117.1:c.3747+141dup	XP_016858606.1:n.3747+141dup
XR_002958896.1:n.3867+141dup
NM_133259.4:c.3825+141dup MANE Select	NP_573566.2:n.3825+141dup