Canonical Allele Identifier: CA319788

Gene: LRPPRC

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43943793C>T , CM000664.2:g.43943793C>T	GRCh38
NC_000002.11:g.44170932C>T , CM000664.1:g.44170932C>T	GRCh37
NC_000002.10:g.44024436C>T	NCBI36
NG_008247.1:g.57213G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409659.6:c.2398G>A	ENSP00000386562.2:p.Gly800Ser
ENST00000447246.2:c.2398G>A	ENSP00000403637.2:p.Gly800Ser
ENST00000681961.1:n.2418G>A
ENST00000682104.1:c.2272G>A	ENSP00000507716.1:p.Gly758Ser
ENST00000682303.1:c.*2184G>A	ENSP00000508325.1:n.*2184G>A
ENST00000682308.1:c.2398G>A	ENSP00000507056.1:p.Gly800Ser
ENST00000682480.1:c.2398G>A	ENSP00000508344.1:p.Gly800Ser
ENST00000682546.1:c.2395G>A	ENSP00000508188.1:p.Gly799Ser
ENST00000682585.1:c.2398G>A	ENSP00000506885.1:p.Gly800Ser
ENST00000682595.1:n.2980G>A
ENST00000682607.1:c.816G>A
ENST00000682779.1:c.2389G>A	ENSP00000507947.1:p.Gly797Ser
ENST00000682845.1:n.1500G>A
ENST00000682885.1:c.2353G>A	ENSP00000508036.1:p.Gly785Ser
ENST00000682933.1:n.2472G>A
ENST00000683072.1:n.2980G>A
ENST00000683125.1:c.2398G>A	ENSP00000507939.1:p.Gly800Ser
ENST00000683213.1:c.2401G>A	ENSP00000507751.1:p.Gly801Ser
ENST00000683220.1:c.2428G>A	ENSP00000507151.1:p.Gly810Ser
ENST00000683329.1:n.3201G>A
ENST00000683346.1:c.*2273G>A	ENSP00000507458.1:n.*2273G>A
ENST00000683459.1:n.2985G>A
ENST00000683590.1:c.2398G>A	ENSP00000506820.1:p.Gly800Ser
ENST00000683623.1:c.2305G>A	ENSP00000507702.1:p.Gly769Ser
ENST00000683645.1:n.2949G>A
ENST00000683694.1:n.1149G>A
ENST00000683796.1:c.*2270G>A	ENSP00000508221.1:n.*2270G>A
ENST00000683802.1:n.5323G>A
ENST00000683833.1:c.2389G>A	ENSP00000506852.1:p.Gly797Ser
ENST00000683989.1:c.2398G>A	ENSP00000507510.1:p.Gly800Ser
ENST00000683994.1:c.2398G>A	ENSP00000507181.1:p.Gly800Ser
ENST00000684290.1:c.*92G>A	ENSP00000507243.1:n.*92G>A
ENST00000684306.1:c.*2311G>A	ENSP00000508384.1:n.*2311G>A
ENST00000684341.1:n.2418G>A
ENST00000684383.1:c.*2036G>A	ENSP00000506863.1:n.*2036G>A
ENST00000684397.1:c.102G>A
ENST00000684619.1:c.*2270G>A	ENSP00000508088.1:n.*2270G>A
ENST00000684743.1:n.3429G>A
ENST00000260665.12:c.2398G>A MANE Select	ENSP00000260665.7:p.Gly800Ser
ENST00000260665.11:c.2398G>A	ENSP00000260665.7:p.Gly800Ser
NM_133259.3:c.2398G>A	NP_573566.2:p.Gly800Ser
XM_006711915.2:c.2320G>A	XP_006711978.1:p.Gly774Ser
XM_006711916.2:c.2398G>A	XP_006711979.1:p.Gly800Ser
XM_011532473.1:c.2398G>A	XP_011530775.1:p.Gly800Ser
XM_011532474.1:c.2398G>A	XP_011530776.1:p.Gly800Ser
XM_006711916.3:c.2398G>A	XP_006711979.1:p.Gly800Ser
XM_017003117.1:c.2320G>A	XP_016858606.1:p.Gly774Ser
XR_002958896.1:n.2440G>A
NM_133259.4:c.2398G>A MANE Select	NP_573566.2:p.Gly800Ser