Canonical Allele Identifier: CA346668034

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44145202T>G (hg19) ; chr2:g.43918063T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43918063T>G , CM000664.2:g.43918063T>G	GRCh38
NC_000002.11:g.44145202T>G , CM000664.1:g.44145202T>G	GRCh37
NC_000002.10:g.43998706T>G	NCBI36
NG_008247.1:g.82943A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.662A>C
ENST00000682295.1:c.303+193A>C	ENSP00000507499.1:n.303+193A>C
ENST00000682303.1:c.*2896A>C	ENSP00000508325.1:n.*2896A>C
ENST00000682308.1:c.3110A>C	ENSP00000507056.1:p.Lys1037Thr
ENST00000682480.1:c.3128A>C	ENSP00000508344.1:p.Lys1043Thr
ENST00000682546.1:c.3107A>C	ENSP00000508188.1:p.Lys1036Thr
ENST00000682585.1:c.3110A>C	ENSP00000506885.1:p.Lys1037Thr
ENST00000682595.1:n.3694A>C
ENST00000682607.1:c.1528A>C
ENST00000682779.1:c.3101A>C	ENSP00000507947.1:p.Lys1034Thr
ENST00000682845.1:n.2212A>C
ENST00000682885.1:c.3065A>C	ENSP00000508036.1:p.Lys1022Thr
ENST00000682933.1:n.3184A>C
ENST00000683072.1:n.3694A>C
ENST00000683080.1:n.729A>C
ENST00000683125.1:c.3218A>C	ENSP00000507939.1:p.Lys1073Thr
ENST00000683213.1:c.3113A>C	ENSP00000507751.1:p.Lys1038Thr
ENST00000683220.1:c.3140A>C	ENSP00000507151.1:p.Lys1047Thr
ENST00000683329.1:n.3913A>C
ENST00000683346.1:c.*2985A>C	ENSP00000507458.1:n.*2985A>C
ENST00000683409.1:n.1717A>C
ENST00000683459.1:n.3697A>C
ENST00000683590.1:c.2897-5505A>C	ENSP00000506820.1:n.2897-5505A>C
ENST00000683623.1:c.3017A>C	ENSP00000507702.1:p.Lys1006Thr
ENST00000683645.1:n.3661A>C
ENST00000683796.1:c.*2982A>C	ENSP00000508221.1:n.*2982A>C
ENST00000683802.1:n.6035A>C
ENST00000683833.1:c.3101A>C	ENSP00000506852.1:p.Lys1034Thr
ENST00000683994.1:c.3110A>C	ENSP00000507181.1:p.Lys1037Thr
ENST00000684290.1:c.*646A>C	ENSP00000507243.1:n.*646A>C
ENST00000684306.1:c.*3023A>C	ENSP00000508384.1:n.*3023A>C
ENST00000684341.1:n.3130A>C
ENST00000684383.1:c.*2748A>C	ENSP00000506863.1:n.*2748A>C
ENST00000684619.1:c.*2982A>C	ENSP00000508088.1:n.*2982A>C
ENST00000684705.1:n.231A>C
ENST00000684743.1:n.4141A>C
ENST00000260665.12:c.3110A>C MANE Select	ENSP00000260665.7:p.Lys1037Thr
ENST00000260665.11:c.3110A>C	ENSP00000260665.7:p.Lys1037Thr
NM_133259.3:c.3110A>C	NP_573566.2:p.Lys1037Thr
XM_006711915.2:c.3032A>C	XP_006711978.1:p.Lys1011Thr
XM_006711916.2:c.3110A>C	XP_006711979.1:p.Lys1037Thr
XM_011532473.1:c.3110A>C	XP_011530775.1:p.Lys1037Thr
XM_011532474.1:c.3110A>C	XP_011530776.1:p.Lys1037Thr
XM_006711916.3:c.3110A>C	XP_006711979.1:p.Lys1037Thr
XM_017003117.1:c.3032A>C	XP_016858606.1:p.Lys1011Thr
XR_002958896.1:n.3152A>C
NM_133259.4:c.3110A>C MANE Select	NP_573566.2:p.Lys1037Thr