Canonical Allele Identifier: CA425908494

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44145216T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43918077T>C , CM000664.2:g.43918077T>C	GRCh38
NC_000002.11:g.44145216T>C , CM000664.1:g.44145216T>C	GRCh37
NC_000002.10:g.43998720T>C	NCBI36
NG_008247.1:g.82929A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.648A>G
ENST00000682295.1:c.303+179A>G	ENSP00000507499.1:n.303+179A>G
ENST00000682303.1:c.*2882A>G	ENSP00000508325.1:n.*2882A>G
ENST00000682308.1:c.3096A>G	ENSP00000507056.1:p.Glu1032=
ENST00000682480.1:c.3114A>G	ENSP00000508344.1:p.Glu1038=
ENST00000682546.1:c.3093A>G	ENSP00000508188.1:p.Glu1031=
ENST00000682585.1:c.3096A>G	ENSP00000506885.1:p.Glu1032=
ENST00000682595.1:n.3680A>G
ENST00000682607.1:c.1514A>G
ENST00000682779.1:c.3087A>G	ENSP00000507947.1:p.Glu1029=
ENST00000682845.1:n.2198A>G
ENST00000682885.1:c.3051A>G	ENSP00000508036.1:p.Glu1017=
ENST00000682933.1:n.3170A>G
ENST00000683072.1:n.3680A>G
ENST00000683080.1:n.715A>G
ENST00000683125.1:c.3204A>G	ENSP00000507939.1:p.Glu1068=
ENST00000683213.1:c.3099A>G	ENSP00000507751.1:p.Glu1033=
ENST00000683220.1:c.3126A>G	ENSP00000507151.1:p.Glu1042=
ENST00000683329.1:n.3899A>G
ENST00000683346.1:c.*2971A>G	ENSP00000507458.1:n.*2971A>G
ENST00000683409.1:n.1703A>G
ENST00000683459.1:n.3683A>G
ENST00000683590.1:c.2897-5519A>G	ENSP00000506820.1:n.2897-5519A>G
ENST00000683623.1:c.3003A>G	ENSP00000507702.1:p.Glu1001=
ENST00000683645.1:n.3647A>G
ENST00000683796.1:c.*2968A>G	ENSP00000508221.1:n.*2968A>G
ENST00000683802.1:n.6021A>G
ENST00000683833.1:c.3087A>G	ENSP00000506852.1:p.Glu1029=
ENST00000683994.1:c.3096A>G	ENSP00000507181.1:p.Glu1032=
ENST00000684290.1:c.*632A>G	ENSP00000507243.1:n.*632A>G
ENST00000684306.1:c.*3009A>G	ENSP00000508384.1:n.*3009A>G
ENST00000684341.1:n.3116A>G
ENST00000684383.1:c.*2734A>G	ENSP00000506863.1:n.*2734A>G
ENST00000684619.1:c.*2968A>G	ENSP00000508088.1:n.*2968A>G
ENST00000684705.1:n.217A>G
ENST00000684743.1:n.4127A>G
ENST00000260665.12:c.3096A>G MANE Select	ENSP00000260665.7:p.Glu1032=
ENST00000260665.11:c.3096A>G	ENSP00000260665.7:p.Glu1032=
NM_133259.3:c.3096A>G	NP_573566.2:p.Glu1032=
XM_006711915.2:c.3018A>G	XP_006711978.1:p.Glu1006=
XM_006711916.2:c.3096A>G	XP_006711979.1:p.Glu1032=
XM_011532473.1:c.3096A>G	XP_011530775.1:p.Glu1032=
XM_011532474.1:c.3096A>G	XP_011530776.1:p.Glu1032=
XM_006711916.3:c.3096A>G	XP_006711979.1:p.Glu1032=
XM_017003117.1:c.3018A>G	XP_016858606.1:p.Glu1006=
XR_002958896.1:n.3138A>G
NM_133259.4:c.3096A>G MANE Select	NP_573566.2:p.Glu1032=