Canonical Allele Identifier: CA425909136

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44121766T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43894627T>A , CM000664.2:g.43894627T>A	GRCh38
NC_000002.11:g.44121766T>A , CM000664.1:g.44121766T>A	GRCh37
NC_000002.10:g.43975270T>A	NCBI36
NG_008247.1:g.106379A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419884.6:c.533A>T
ENST00000681993.1:n.1455A>T
ENST00000682154.1:n.1337A>T
ENST00000682303.1:c.*3614A>T	ENSP00000508325.1:n.*3614A>T
ENST00000682308.1:c.3828A>T	ENSP00000507056.1:p.Ala1276=
ENST00000682434.1:n.3458A>T
ENST00000682480.1:c.3921A>T	ENSP00000508344.1:p.Ala1307=
ENST00000682546.1:c.3900A>T	ENSP00000508188.1:p.Ala1300=
ENST00000682585.1:c.*31A>T	ENSP00000506885.1:n.*31A>T
ENST00000682607.1:c.2646A>T
ENST00000682612.1:c.752+2007A>T
ENST00000682696.1:c.3A>T	ENSP00000508411.1:p.Ala1=
ENST00000682779.1:c.3894A>T	ENSP00000507947.1:p.Ala1298=
ENST00000682885.1:c.3858A>T	ENSP00000508036.1:p.Ala1286=
ENST00000682933.1:n.4103A>T
ENST00000683002.1:c.755A>T
ENST00000683072.1:n.4487A>T
ENST00000683080.1:n.1522A>T
ENST00000683096.1:n.2344A>T
ENST00000683125.1:c.4011A>T	ENSP00000507939.1:p.Ala1337=
ENST00000683213.1:c.3906A>T	ENSP00000507751.1:p.Ala1302=
ENST00000683220.1:c.3933A>T	ENSP00000507151.1:p.Ala1311=
ENST00000683329.1:n.4706A>T
ENST00000683346.1:c.*3778A>T	ENSP00000507458.1:n.*3778A>T
ENST00000683409.1:n.2435A>T
ENST00000683459.1:n.4490A>T
ENST00000683590.1:c.3576A>T	ENSP00000506820.1:p.Ala1192=
ENST00000683623.1:c.3810A>T	ENSP00000507702.1:p.Ala1270=
ENST00000683796.1:c.*3700A>T	ENSP00000508221.1:n.*3700A>T
ENST00000683833.1:c.3819A>T	ENSP00000506852.1:p.Ala1273=
ENST00000683994.1:c.*16A>T	ENSP00000507181.1:n.*16A>T
ENST00000684290.1:c.*1364A>T	ENSP00000507243.1:n.*1364A>T
ENST00000684306.1:c.*3816A>T	ENSP00000508384.1:n.*3816A>T
ENST00000684383.1:c.*3541A>T	ENSP00000506863.1:n.*3541A>T
ENST00000684418.1:n.5084A>T
ENST00000684433.1:n.287A>T
ENST00000684454.1:n.7767A>T
ENST00000684619.1:c.*3775A>T	ENSP00000508088.1:n.*3775A>T
ENST00000684743.1:n.6648A>T
ENST00000260665.12:c.3903A>T MANE Select	ENSP00000260665.7:p.Ala1301=
ENST00000260665.11:c.3903A>T	ENSP00000260665.7:p.Ala1301=
ENST00000419884.5:c.144A>T	ENSP00000414207.1:p.Ala48=
ENST00000463456.5:n.2946A>T
NM_133259.3:c.3903A>T	NP_573566.2:p.Ala1301=
XM_006711915.2:c.3825A>T	XP_006711978.1:p.Ala1275=
XM_011532473.1:c.3828A>T	XP_011530775.1:p.Ala1276=
XM_011532474.1:c.3903A>T	XP_011530776.1:p.Ala1301=
XM_017003117.1:c.3750A>T	XP_016858606.1:p.Ala1250=
XR_002958896.1:n.3945A>T
NM_133259.4:c.3903A>T MANE Select	NP_573566.2:p.Ala1301=