Canonical Allele Identifier: CA2493977922

Gene: LRPPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43899235G= , CM000664.2:g.43899235G=	GRCh38
NC_000002.11:g.44126374G= , CM000664.1:g.44126374G=	GRCh37
NC_000002.10:g.43979878G=	NCBI36
NG_008247.1:g.101771C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419884.6:c.240C=
ENST00000472420.6:n.888C=
ENST00000483489.2:n.240C=
ENST00000681993.1:n.1361C=
ENST00000682303.1:c.*3595C=	ENSP00000508325.1:n.*3595C=
ENST00000682308.1:c.3809C=	ENSP00000507056.1:p.Ala1270=
ENST00000682434.1:n.1360C=
ENST00000682480.1:c.3827C=	ENSP00000508344.1:p.Ala1276=
ENST00000682546.1:c.3806C=	ENSP00000508188.1:p.Ala1269=
ENST00000682585.1:c.3809C=	ENSP00000506885.1:p.Ala1270=
ENST00000682595.1:n.4393C=
ENST00000682607.1:c.2227C=
ENST00000682612.1:c.661C=
ENST00000682779.1:c.3800C=	ENSP00000507947.1:p.Ala1267=
ENST00000682885.1:c.3764C=	ENSP00000508036.1:p.Ala1255=
ENST00000682933.1:n.3883C=
ENST00000683002.1:c.661C=
ENST00000683072.1:n.4393C=
ENST00000683080.1:n.1428C=
ENST00000683125.1:c.3917C=	ENSP00000507939.1:p.Ala1306=
ENST00000683213.1:c.3812C=	ENSP00000507751.1:p.Ala1271=
ENST00000683220.1:c.3839C=	ENSP00000507151.1:p.Ala1280=
ENST00000683329.1:n.4612C=
ENST00000683346.1:c.*3684C=	ENSP00000507458.1:n.*3684C=
ENST00000683409.1:n.2416C=
ENST00000683459.1:n.4396C=
ENST00000683528.1:c.737C=
ENST00000683590.1:c.3557C=	ENSP00000506820.1:p.Ala1186=
ENST00000683623.1:c.3716C=	ENSP00000507702.1:p.Ala1239=
ENST00000683645.1:n.4360C=
ENST00000683796.1:c.*3681C=	ENSP00000508221.1:n.*3681C=
ENST00000683802.1:n.6734C=
ENST00000683833.1:c.3800C=	ENSP00000506852.1:p.Ala1267=
ENST00000683994.1:c.3809C=	ENSP00000507181.1:p.Ala1270=
ENST00000684290.1:c.*1345C=	ENSP00000507243.1:n.*1345C=
ENST00000684306.1:c.*3722C=	ENSP00000508384.1:n.*3722C=
ENST00000684341.1:n.3829C=
ENST00000684383.1:c.*3447C=	ENSP00000506863.1:n.*3447C=
ENST00000684418.1:n.4990C=
ENST00000684433.1:n.193C=
ENST00000684454.1:n.3159C=
ENST00000684619.1:c.*3681C=	ENSP00000508088.1:n.*3681C=
ENST00000684743.1:n.6554C=
ENST00000260665.12:c.3809C= MANE Select	ENSP00000260665.7:p.Ala1270=
ENST00000260665.11:c.3809C=	ENSP00000260665.7:p.Ala1270=
ENST00000419884.5:c.50C=	ENSP00000414207.1:p.Ala17=
ENST00000463456.5:n.2852C=
ENST00000472420.5:n.206C=
ENST00000483489.1:n.283C=
NM_133259.3:c.3809C=	NP_573566.2:p.Ala1270=
XM_006711915.2:c.3731C=	XP_006711978.1:p.Ala1244=
XM_011532473.1:c.3809C=	XP_011530775.1:p.Ala1270=
XM_011532474.1:c.3809C=	XP_011530776.1:p.Ala1270=
XM_017003117.1:c.3731C=	XP_016858606.1:p.Ala1244=
XR_002958896.1:n.3851C=
NM_133259.4:c.3809C= MANE Select	NP_573566.2:p.Ala1270=