Canonical Allele Identifier: CA346668461

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44145429T>C (hg19) ; chr2:g.43918290T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43918290T>C , CM000664.2:g.43918290T>C	GRCh38
NC_000002.11:g.44145429T>C , CM000664.1:g.44145429T>C	GRCh37
NC_000002.10:g.43998933T>C	NCBI36
NG_008247.1:g.82716A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.557A>G
ENST00000682295.1:c.269A>G	ENSP00000507499.1:p.Glu90Gly
ENST00000682303.1:c.*2791A>G	ENSP00000508325.1:n.*2791A>G
ENST00000682308.1:c.3005A>G	ENSP00000507056.1:p.Glu1002Gly
ENST00000682480.1:c.3005A>G	ENSP00000508344.1:p.Glu1002Gly
ENST00000682546.1:c.3002A>G	ENSP00000508188.1:p.Glu1001Gly
ENST00000682585.1:c.3005A>G	ENSP00000506885.1:p.Glu1002Gly
ENST00000682595.1:n.3589A>G
ENST00000682607.1:c.1423A>G
ENST00000682779.1:c.2996A>G	ENSP00000507947.1:p.Glu999Gly
ENST00000682845.1:n.2107A>G
ENST00000682885.1:c.2960A>G	ENSP00000508036.1:p.Glu987Gly
ENST00000682933.1:n.3079A>G
ENST00000683072.1:n.3589A>G
ENST00000683080.1:n.624A>G
ENST00000683125.1:c.3113A>G	ENSP00000507939.1:p.Glu1038Gly
ENST00000683213.1:c.3008A>G	ENSP00000507751.1:p.Glu1003Gly
ENST00000683220.1:c.3035A>G	ENSP00000507151.1:p.Glu1012Gly
ENST00000683236.1:c.335A>G	ENSP00000506891.1:n.335A>G
ENST00000683329.1:n.3808A>G
ENST00000683346.1:c.*2880A>G	ENSP00000507458.1:n.*2880A>G
ENST00000683409.1:n.1612A>G
ENST00000683459.1:n.3592A>G
ENST00000683590.1:c.2897-5732A>G	ENSP00000506820.1:n.2897-5732A>G
ENST00000683623.1:c.2912A>G	ENSP00000507702.1:p.Glu971Gly
ENST00000683645.1:n.3556A>G
ENST00000683796.1:c.*2877A>G	ENSP00000508221.1:n.*2877A>G
ENST00000683802.1:n.5930A>G
ENST00000683833.1:c.2996A>G	ENSP00000506852.1:p.Glu999Gly
ENST00000683994.1:c.3005A>G	ENSP00000507181.1:p.Glu1002Gly
ENST00000684290.1:c.*541A>G	ENSP00000507243.1:n.*541A>G
ENST00000684306.1:c.*2918A>G	ENSP00000508384.1:n.*2918A>G
ENST00000684341.1:n.3025A>G
ENST00000684383.1:c.*2643A>G	ENSP00000506863.1:n.*2643A>G
ENST00000684619.1:c.*2877A>G	ENSP00000508088.1:n.*2877A>G
ENST00000684705.1:n.126A>G
ENST00000684743.1:n.4036A>G
ENST00000260665.12:c.3005A>G MANE Select	ENSP00000260665.7:p.Glu1002Gly
ENST00000260665.11:c.3005A>G	ENSP00000260665.7:p.Glu1002Gly
NM_133259.3:c.3005A>G	NP_573566.2:p.Glu1002Gly
XM_006711915.2:c.2927A>G	XP_006711978.1:p.Glu976Gly
XM_006711916.2:c.3005A>G	XP_006711979.1:p.Glu1002Gly
XM_011532473.1:c.3005A>G	XP_011530775.1:p.Glu1002Gly
XM_011532474.1:c.3005A>G	XP_011530776.1:p.Glu1002Gly
XM_006711916.3:c.3005A>G	XP_006711979.1:p.Glu1002Gly
XM_017003117.1:c.2927A>G	XP_016858606.1:p.Glu976Gly
XR_002958896.1:n.3047A>G
NM_133259.4:c.3005A>G MANE Select	NP_573566.2:p.Glu1002Gly