Canonical Allele Identifier: CA346668537

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44145464T>G (hg19) ; chr2:g.43918325T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43918325T>G , CM000664.2:g.43918325T>G	GRCh38
NC_000002.11:g.44145464T>G , CM000664.1:g.44145464T>G	GRCh37
NC_000002.10:g.43998968T>G	NCBI36
NG_008247.1:g.82681A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.522A>C
ENST00000682295.1:c.234A>C	ENSP00000507499.1:p.Glu78Asp
ENST00000682303.1:c.*2756A>C	ENSP00000508325.1:n.*2756A>C
ENST00000682308.1:c.2970A>C	ENSP00000507056.1:p.Glu990Asp
ENST00000682480.1:c.2970A>C	ENSP00000508344.1:p.Glu990Asp
ENST00000682546.1:c.2967A>C	ENSP00000508188.1:p.Glu989Asp
ENST00000682585.1:c.2970A>C	ENSP00000506885.1:p.Glu990Asp
ENST00000682595.1:n.3554A>C
ENST00000682607.1:c.1388A>C
ENST00000682779.1:c.2961A>C	ENSP00000507947.1:p.Glu987Asp
ENST00000682845.1:n.2072A>C
ENST00000682885.1:c.2925A>C	ENSP00000508036.1:p.Glu975Asp
ENST00000682933.1:n.3044A>C
ENST00000683072.1:n.3554A>C
ENST00000683080.1:n.589A>C
ENST00000683125.1:c.3078A>C	ENSP00000507939.1:p.Glu1026Asp
ENST00000683213.1:c.2973A>C	ENSP00000507751.1:p.Glu991Asp
ENST00000683220.1:c.3000A>C	ENSP00000507151.1:p.Glu1000Asp
ENST00000683236.1:c.300A>C	ENSP00000506891.1:n.300A>C
ENST00000683329.1:n.3773A>C
ENST00000683346.1:c.*2845A>C	ENSP00000507458.1:n.*2845A>C
ENST00000683409.1:n.1577A>C
ENST00000683459.1:n.3557A>C
ENST00000683590.1:c.2897-5767A>C	ENSP00000506820.1:n.2897-5767A>C
ENST00000683623.1:c.2877A>C	ENSP00000507702.1:p.Glu959Asp
ENST00000683645.1:n.3521A>C
ENST00000683796.1:c.*2842A>C	ENSP00000508221.1:n.*2842A>C
ENST00000683802.1:n.5895A>C
ENST00000683833.1:c.2961A>C	ENSP00000506852.1:p.Glu987Asp
ENST00000683994.1:c.2970A>C	ENSP00000507181.1:p.Glu990Asp
ENST00000684290.1:c.*506A>C	ENSP00000507243.1:n.*506A>C
ENST00000684306.1:c.*2883A>C	ENSP00000508384.1:n.*2883A>C
ENST00000684341.1:n.2990A>C
ENST00000684383.1:c.*2608A>C	ENSP00000506863.1:n.*2608A>C
ENST00000684619.1:c.*2842A>C	ENSP00000508088.1:n.*2842A>C
ENST00000684705.1:n.91A>C
ENST00000684743.1:n.4001A>C
ENST00000260665.12:c.2970A>C MANE Select	ENSP00000260665.7:p.Glu990Asp
ENST00000260665.11:c.2970A>C	ENSP00000260665.7:p.Glu990Asp
NM_133259.3:c.2970A>C	NP_573566.2:p.Glu990Asp
XM_006711915.2:c.2892A>C	XP_006711978.1:p.Glu964Asp
XM_006711916.2:c.2970A>C	XP_006711979.1:p.Glu990Asp
XM_011532473.1:c.2970A>C	XP_011530775.1:p.Glu990Asp
XM_011532474.1:c.2970A>C	XP_011530776.1:p.Glu990Asp
XM_006711916.3:c.2970A>C	XP_006711979.1:p.Glu990Asp
XM_017003117.1:c.2892A>C	XP_016858606.1:p.Glu964Asp
XR_002958896.1:n.3012A>C
NM_133259.4:c.2970A>C MANE Select	NP_573566.2:p.Glu990Asp