Canonical Allele Identifier: CA2493981265

Gene: LRPPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43905763T= , CM000664.2:g.43905763T=	GRCh38
NC_000002.11:g.44132902T= , CM000664.1:g.44132902T=	GRCh37
NC_000002.10:g.43986406T=	NCBI36
NG_008247.1:g.95243A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000472420.6:n.372A=
ENST00000681993.1:n.845A=
ENST00000682295.1:c.448A=	ENSP00000507499.1:n.448A=
ENST00000682303.1:c.*3079A=	ENSP00000508325.1:n.*3079A=
ENST00000682308.1:c.3293A=	ENSP00000507056.1:p.Lys1098=
ENST00000682480.1:c.3311A=	ENSP00000508344.1:p.Lys1104=
ENST00000682546.1:c.3290A=	ENSP00000508188.1:p.Lys1097=
ENST00000682585.1:c.3293A=	ENSP00000506885.1:p.Lys1098=
ENST00000682595.1:n.3877A=
ENST00000682607.1:c.1711A=
ENST00000682612.1:c.145A=
ENST00000682779.1:c.3284A=	ENSP00000507947.1:p.Lys1095=
ENST00000682845.1:n.2395A=
ENST00000682885.1:c.3248A=	ENSP00000508036.1:p.Lys1083=
ENST00000682933.1:n.3367A=
ENST00000683002.1:c.145A=
ENST00000683072.1:n.3877A=
ENST00000683080.1:n.912A=
ENST00000683125.1:c.3401A=	ENSP00000507939.1:p.Lys1134=
ENST00000683213.1:c.3296A=	ENSP00000507751.1:p.Lys1099=
ENST00000683220.1:c.3323A=	ENSP00000507151.1:p.Lys1108=
ENST00000683329.1:n.4096A=
ENST00000683346.1:c.*3168A=	ENSP00000507458.1:n.*3168A=
ENST00000683409.1:n.1900A=
ENST00000683459.1:n.3880A=
ENST00000683528.1:c.145A=
ENST00000683590.1:c.3041A=	ENSP00000506820.1:p.Lys1014=
ENST00000683623.1:c.3200A=	ENSP00000507702.1:p.Lys1067=
ENST00000683645.1:n.3844A=
ENST00000683796.1:c.*3165A=	ENSP00000508221.1:n.*3165A=
ENST00000683802.1:n.6218A=
ENST00000683833.1:c.3284A=	ENSP00000506852.1:p.Lys1095=
ENST00000683994.1:c.3293A=	ENSP00000507181.1:p.Lys1098=
ENST00000684290.1:c.*829A=	ENSP00000507243.1:n.*829A=
ENST00000684306.1:c.*3206A=	ENSP00000508384.1:n.*3206A=
ENST00000684341.1:n.3313A=
ENST00000684383.1:c.*2931A=	ENSP00000506863.1:n.*2931A=
ENST00000684418.1:n.4474A=
ENST00000684454.1:n.2643A=
ENST00000684619.1:c.*3165A=	ENSP00000508088.1:n.*3165A=
ENST00000684743.1:n.4324A=
ENST00000260665.12:c.3293A= MANE Select	ENSP00000260665.7:p.Lys1098=
ENST00000260665.11:c.3293A=	ENSP00000260665.7:p.Lys1098=
NM_133259.3:c.3293A=	NP_573566.2:p.Lys1098=
XM_006711915.2:c.3215A=	XP_006711978.1:p.Lys1072=
XM_011532473.1:c.3293A=	XP_011530775.1:p.Lys1098=
XM_011532474.1:c.3293A=	XP_011530776.1:p.Lys1098=
XM_017003117.1:c.3215A=	XP_016858606.1:p.Lys1072=
XR_002958896.1:n.3335A=
NM_133259.4:c.3293A= MANE Select	NP_573566.2:p.Lys1098=