Canonical Allele Identifier: CA425909656

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44170828T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43943689T>C , CM000664.2:g.43943689T>C	GRCh38
NC_000002.11:g.44170828T>C , CM000664.1:g.44170828T>C	GRCh37
NC_000002.10:g.44024332T>C	NCBI36
NG_008247.1:g.57317A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000409659.6:c.2502A>G	ENSP00000386562.2:p.Glu834=
ENST00000447246.2:c.2502A>G	ENSP00000403637.2:p.Glu834=
ENST00000681961.1:n.2522A>G
ENST00000682104.1:c.2376A>G	ENSP00000507716.1:p.Glu792=
ENST00000682303.1:c.*2288A>G	ENSP00000508325.1:n.*2288A>G
ENST00000682308.1:c.2502A>G	ENSP00000507056.1:p.Glu834=
ENST00000682480.1:c.2502A>G	ENSP00000508344.1:p.Glu834=
ENST00000682546.1:c.2499A>G	ENSP00000508188.1:p.Glu833=
ENST00000682585.1:c.2502A>G	ENSP00000506885.1:p.Glu834=
ENST00000682595.1:n.3084A>G
ENST00000682607.1:c.920A>G
ENST00000682779.1:c.2493A>G	ENSP00000507947.1:p.Glu831=
ENST00000682845.1:n.1604A>G
ENST00000682885.1:c.2457A>G	ENSP00000508036.1:p.Glu819=
ENST00000682933.1:n.2576A>G
ENST00000683072.1:n.3084A>G
ENST00000683125.1:c.2502A>G	ENSP00000507939.1:p.Glu834=
ENST00000683213.1:c.2505A>G	ENSP00000507751.1:p.Glu835=
ENST00000683220.1:c.2532A>G	ENSP00000507151.1:p.Glu844=
ENST00000683329.1:n.3305A>G
ENST00000683346.1:c.*2377A>G	ENSP00000507458.1:n.*2377A>G
ENST00000683459.1:n.3089A>G
ENST00000683590.1:c.2502A>G	ENSP00000506820.1:p.Glu834=
ENST00000683623.1:c.2409A>G	ENSP00000507702.1:p.Glu803=
ENST00000683645.1:n.3053A>G
ENST00000683694.1:n.1253A>G
ENST00000683796.1:c.*2374A>G	ENSP00000508221.1:n.*2374A>G
ENST00000683802.1:n.5427A>G
ENST00000683833.1:c.2493A>G	ENSP00000506852.1:p.Glu831=
ENST00000683989.1:c.2502A>G	ENSP00000507510.1:p.Glu834=
ENST00000683994.1:c.2502A>G	ENSP00000507181.1:p.Glu834=
ENST00000684290.1:c.*196A>G	ENSP00000507243.1:n.*196A>G
ENST00000684306.1:c.*2415A>G	ENSP00000508384.1:n.*2415A>G
ENST00000684341.1:n.2522A>G
ENST00000684383.1:c.*2140A>G	ENSP00000506863.1:n.*2140A>G
ENST00000684397.1:c.206A>G
ENST00000684619.1:c.*2374A>G	ENSP00000508088.1:n.*2374A>G
ENST00000684743.1:n.3533A>G
ENST00000260665.12:c.2502A>G MANE Select	ENSP00000260665.7:p.Glu834=
ENST00000260665.11:c.2502A>G	ENSP00000260665.7:p.Glu834=
NM_133259.3:c.2502A>G	NP_573566.2:p.Glu834=
XM_006711915.2:c.2424A>G	XP_006711978.1:p.Glu808=
XM_006711916.2:c.2502A>G	XP_006711979.1:p.Glu834=
XM_011532473.1:c.2502A>G	XP_011530775.1:p.Glu834=
XM_011532474.1:c.2502A>G	XP_011530776.1:p.Glu834=
XM_006711916.3:c.2502A>G	XP_006711979.1:p.Glu834=
XM_017003117.1:c.2424A>G	XP_016858606.1:p.Glu808=
XR_002958896.1:n.2544A>G
NM_133259.4:c.2502A>G MANE Select	NP_573566.2:p.Glu834=