Canonical Allele Identifier: CA2493977934

Gene: LRPPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43899269G= , CM000664.2:g.43899269G=	GRCh38
NC_000002.11:g.44126408G= , CM000664.1:g.44126408G=	GRCh37
NC_000002.10:g.43979912G=	NCBI36
NG_008247.1:g.101737C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419884.6:c.206C=
ENST00000472420.6:n.854C=
ENST00000483489.2:n.206C=
ENST00000681993.1:n.1327C=
ENST00000682303.1:c.*3561C=	ENSP00000508325.1:n.*3561C=
ENST00000682308.1:c.3775C=	ENSP00000507056.1:p.Leu1259=
ENST00000682434.1:n.1326C=
ENST00000682480.1:c.3793C=	ENSP00000508344.1:p.Leu1265=
ENST00000682546.1:c.3772C=	ENSP00000508188.1:p.Leu1258=
ENST00000682585.1:c.3775C=	ENSP00000506885.1:p.Leu1259=
ENST00000682595.1:n.4359C=
ENST00000682607.1:c.2193C=
ENST00000682612.1:c.627C=
ENST00000682779.1:c.3766C=	ENSP00000507947.1:p.Leu1256=
ENST00000682845.1:n.2877C=
ENST00000682885.1:c.3730C=	ENSP00000508036.1:p.Leu1244=
ENST00000682933.1:n.3849C=
ENST00000683002.1:c.627C=
ENST00000683072.1:n.4359C=
ENST00000683080.1:n.1394C=
ENST00000683125.1:c.3883C=	ENSP00000507939.1:p.Leu1295=
ENST00000683213.1:c.3778C=	ENSP00000507751.1:p.Leu1260=
ENST00000683220.1:c.3805C=	ENSP00000507151.1:p.Leu1269=
ENST00000683329.1:n.4578C=
ENST00000683346.1:c.*3650C=	ENSP00000507458.1:n.*3650C=
ENST00000683409.1:n.2382C=
ENST00000683459.1:n.4362C=
ENST00000683528.1:c.703C=
ENST00000683590.1:c.3523C=	ENSP00000506820.1:p.Leu1175=
ENST00000683623.1:c.3682C=	ENSP00000507702.1:p.Leu1228=
ENST00000683645.1:n.4326C=
ENST00000683796.1:c.*3647C=	ENSP00000508221.1:n.*3647C=
ENST00000683802.1:n.6700C=
ENST00000683833.1:c.3766C=	ENSP00000506852.1:p.Leu1256=
ENST00000683994.1:c.3775C=	ENSP00000507181.1:p.Leu1259=
ENST00000684290.1:c.*1311C=	ENSP00000507243.1:n.*1311C=
ENST00000684306.1:c.*3688C=	ENSP00000508384.1:n.*3688C=
ENST00000684341.1:n.3795C=
ENST00000684383.1:c.*3413C=	ENSP00000506863.1:n.*3413C=
ENST00000684418.1:n.4956C=
ENST00000684433.1:n.159C=
ENST00000684454.1:n.3125C=
ENST00000684619.1:c.*3647C=	ENSP00000508088.1:n.*3647C=
ENST00000684743.1:n.6520C=
ENST00000260665.12:c.3775C= MANE Select	ENSP00000260665.7:p.Leu1259=
ENST00000260665.11:c.3775C=	ENSP00000260665.7:p.Leu1259=
ENST00000419884.5:c.16C=	ENSP00000414207.1:p.Leu6=
ENST00000463456.5:n.2818C=
ENST00000472420.5:n.172C=
ENST00000483489.1:n.249C=
NM_133259.3:c.3775C=	NP_573566.2:p.Leu1259=
XM_006711915.2:c.3697C=	XP_006711978.1:p.Leu1233=
XM_011532473.1:c.3775C=	XP_011530775.1:p.Leu1259=
XM_011532474.1:c.3775C=	XP_011530776.1:p.Leu1259=
XM_017003117.1:c.3697C=	XP_016858606.1:p.Leu1233=
XR_002958896.1:n.3817C=
NM_133259.4:c.3775C= MANE Select	NP_573566.2:p.Leu1259=