Canonical Allele Identifier: CA2493988111

Gene: LRPPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43918094A= , CM000664.2:g.43918094A=	GRCh38
NC_000002.11:g.44145233A= , CM000664.1:g.44145233A=	GRCh37
NC_000002.10:g.43998737A=	NCBI36
NG_008247.1:g.82912T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.631T=
ENST00000682295.1:c.303+162T=	ENSP00000507499.1:n.303+162T=
ENST00000682303.1:c.*2865T=	ENSP00000508325.1:n.*2865T=
ENST00000682308.1:c.3079T=	ENSP00000507056.1:p.Ser1027=
ENST00000682480.1:c.3097T=	ENSP00000508344.1:p.Ser1033=
ENST00000682546.1:c.3076T=	ENSP00000508188.1:p.Ser1026=
ENST00000682585.1:c.3079T=	ENSP00000506885.1:p.Ser1027=
ENST00000682595.1:n.3663T=
ENST00000682607.1:c.1497T=
ENST00000682779.1:c.3070T=	ENSP00000507947.1:p.Ser1024=
ENST00000682845.1:n.2181T=
ENST00000682885.1:c.3034T=	ENSP00000508036.1:p.Ser1012=
ENST00000682933.1:n.3153T=
ENST00000683072.1:n.3663T=
ENST00000683080.1:n.698T=
ENST00000683125.1:c.3187T=	ENSP00000507939.1:p.Ser1063=
ENST00000683213.1:c.3082T=	ENSP00000507751.1:p.Ser1028=
ENST00000683220.1:c.3109T=	ENSP00000507151.1:p.Ser1037=
ENST00000683329.1:n.3882T=
ENST00000683346.1:c.*2954T=	ENSP00000507458.1:n.*2954T=
ENST00000683409.1:n.1686T=
ENST00000683459.1:n.3666T=
ENST00000683590.1:c.2897-5536T=	ENSP00000506820.1:n.2897-5536T=
ENST00000683623.1:c.2986T=	ENSP00000507702.1:p.Ser996=
ENST00000683645.1:n.3630T=
ENST00000683796.1:c.*2951T=	ENSP00000508221.1:n.*2951T=
ENST00000683802.1:n.6004T=
ENST00000683833.1:c.3070T=	ENSP00000506852.1:p.Ser1024=
ENST00000683994.1:c.3079T=	ENSP00000507181.1:p.Ser1027=
ENST00000684290.1:c.*615T=	ENSP00000507243.1:n.*615T=
ENST00000684306.1:c.*2992T=	ENSP00000508384.1:n.*2992T=
ENST00000684341.1:n.3099T=
ENST00000684383.1:c.*2717T=	ENSP00000506863.1:n.*2717T=
ENST00000684619.1:c.*2951T=	ENSP00000508088.1:n.*2951T=
ENST00000684705.1:n.200T=
ENST00000684743.1:n.4110T=
ENST00000260665.12:c.3079T= MANE Select	ENSP00000260665.7:p.Ser1027=
ENST00000260665.11:c.3079T=	ENSP00000260665.7:p.Ser1027=
NM_133259.3:c.3079T=	NP_573566.2:p.Ser1027=
XM_006711915.2:c.3001T=	XP_006711978.1:p.Ser1001=
XM_006711916.2:c.3079T=	XP_006711979.1:p.Ser1027=
XM_011532473.1:c.3079T=	XP_011530775.1:p.Ser1027=
XM_011532474.1:c.3079T=	XP_011530776.1:p.Ser1027=
XM_006711916.3:c.3079T=	XP_006711979.1:p.Ser1027=
XM_017003117.1:c.3001T=	XP_016858606.1:p.Ser1001=
XR_002958896.1:n.3121T=
NM_133259.4:c.3079T= MANE Select	NP_573566.2:p.Ser1027=