Canonical Allele Identifier: CA346668114

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44145217T>A (hg19) ; chr2:g.43918078T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43918078T>A , CM000664.2:g.43918078T>A	GRCh38
NC_000002.11:g.44145217T>A , CM000664.1:g.44145217T>A	GRCh37
NC_000002.10:g.43998721T>A	NCBI36
NG_008247.1:g.82928A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.647A>T
ENST00000682295.1:c.303+178A>T	ENSP00000507499.1:n.303+178A>T
ENST00000682303.1:c.*2881A>T	ENSP00000508325.1:n.*2881A>T
ENST00000682308.1:c.3095A>T	ENSP00000507056.1:p.Glu1032Val
ENST00000682480.1:c.3113A>T	ENSP00000508344.1:p.Glu1038Val
ENST00000682546.1:c.3092A>T	ENSP00000508188.1:p.Glu1031Val
ENST00000682585.1:c.3095A>T	ENSP00000506885.1:p.Glu1032Val
ENST00000682595.1:n.3679A>T
ENST00000682607.1:c.1513A>T
ENST00000682779.1:c.3086A>T	ENSP00000507947.1:p.Glu1029Val
ENST00000682845.1:n.2197A>T
ENST00000682885.1:c.3050A>T	ENSP00000508036.1:p.Glu1017Val
ENST00000682933.1:n.3169A>T
ENST00000683072.1:n.3679A>T
ENST00000683080.1:n.714A>T
ENST00000683125.1:c.3203A>T	ENSP00000507939.1:p.Glu1068Val
ENST00000683213.1:c.3098A>T	ENSP00000507751.1:p.Glu1033Val
ENST00000683220.1:c.3125A>T	ENSP00000507151.1:p.Glu1042Val
ENST00000683329.1:n.3898A>T
ENST00000683346.1:c.*2970A>T	ENSP00000507458.1:n.*2970A>T
ENST00000683409.1:n.1702A>T
ENST00000683459.1:n.3682A>T
ENST00000683590.1:c.2897-5520A>T	ENSP00000506820.1:n.2897-5520A>T
ENST00000683623.1:c.3002A>T	ENSP00000507702.1:p.Glu1001Val
ENST00000683645.1:n.3646A>T
ENST00000683796.1:c.*2967A>T	ENSP00000508221.1:n.*2967A>T
ENST00000683802.1:n.6020A>T
ENST00000683833.1:c.3086A>T	ENSP00000506852.1:p.Glu1029Val
ENST00000683994.1:c.3095A>T	ENSP00000507181.1:p.Glu1032Val
ENST00000684290.1:c.*631A>T	ENSP00000507243.1:n.*631A>T
ENST00000684306.1:c.*3008A>T	ENSP00000508384.1:n.*3008A>T
ENST00000684341.1:n.3115A>T
ENST00000684383.1:c.*2733A>T	ENSP00000506863.1:n.*2733A>T
ENST00000684619.1:c.*2967A>T	ENSP00000508088.1:n.*2967A>T
ENST00000684705.1:n.216A>T
ENST00000684743.1:n.4126A>T
ENST00000260665.12:c.3095A>T MANE Select	ENSP00000260665.7:p.Glu1032Val
ENST00000260665.11:c.3095A>T	ENSP00000260665.7:p.Glu1032Val
NM_133259.3:c.3095A>T	NP_573566.2:p.Glu1032Val
XM_006711915.2:c.3017A>T	XP_006711978.1:p.Glu1006Val
XM_006711916.2:c.3095A>T	XP_006711979.1:p.Glu1032Val
XM_011532473.1:c.3095A>T	XP_011530775.1:p.Glu1032Val
XM_011532474.1:c.3095A>T	XP_011530776.1:p.Glu1032Val
XM_006711916.3:c.3095A>T	XP_006711979.1:p.Glu1032Val
XM_017003117.1:c.3017A>T	XP_016858606.1:p.Glu1006Val
XR_002958896.1:n.3137A>T
NM_133259.4:c.3095A>T MANE Select	NP_573566.2:p.Glu1032Val