Canonical Allele Identifier: CA346668673

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44145528C>T (hg19) ; chr2:g.43918389C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43918389C>T , CM000664.2:g.43918389C>T	GRCh38
NC_000002.11:g.44145528C>T , CM000664.1:g.44145528C>T	GRCh37
NC_000002.10:g.43999032C>T	NCBI36
NG_008247.1:g.82617G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.458G>A
ENST00000682295.1:c.170G>A	ENSP00000507499.1:p.Gly57Asp
ENST00000682303.1:c.*2692G>A	ENSP00000508325.1:n.*2692G>A
ENST00000682308.1:c.2906G>A	ENSP00000507056.1:p.Gly969Asp
ENST00000682480.1:c.2906G>A	ENSP00000508344.1:p.Gly969Asp
ENST00000682546.1:c.2903G>A	ENSP00000508188.1:p.Gly968Asp
ENST00000682585.1:c.2906G>A	ENSP00000506885.1:p.Gly969Asp
ENST00000682595.1:n.3490G>A
ENST00000682607.1:c.1324G>A
ENST00000682779.1:c.2897G>A	ENSP00000507947.1:p.Gly966Asp
ENST00000682845.1:n.2008G>A
ENST00000682885.1:c.2861G>A	ENSP00000508036.1:p.Gly954Asp
ENST00000682933.1:n.2980G>A
ENST00000683072.1:n.3490G>A
ENST00000683080.1:n.525G>A
ENST00000683125.1:c.3014G>A	ENSP00000507939.1:p.Gly1005Asp
ENST00000683213.1:c.2909G>A	ENSP00000507751.1:p.Gly970Asp
ENST00000683220.1:c.2936G>A	ENSP00000507151.1:p.Gly979Asp
ENST00000683236.1:c.236G>A	ENSP00000506891.1:n.236G>A
ENST00000683329.1:n.3709G>A
ENST00000683346.1:c.*2781G>A	ENSP00000507458.1:n.*2781G>A
ENST00000683409.1:n.1513G>A
ENST00000683459.1:n.3493G>A
ENST00000683590.1:c.2897-5831G>A	ENSP00000506820.1:n.2897-5831G>A
ENST00000683623.1:c.2813G>A	ENSP00000507702.1:p.Gly938Asp
ENST00000683645.1:n.3457G>A
ENST00000683796.1:c.*2778G>A	ENSP00000508221.1:n.*2778G>A
ENST00000683802.1:n.5831G>A
ENST00000683833.1:c.2897G>A	ENSP00000506852.1:p.Gly966Asp
ENST00000683994.1:c.2906G>A	ENSP00000507181.1:p.Gly969Asp
ENST00000684290.1:c.*442G>A	ENSP00000507243.1:n.*442G>A
ENST00000684306.1:c.*2819G>A	ENSP00000508384.1:n.*2819G>A
ENST00000684341.1:n.2926G>A
ENST00000684383.1:c.*2544G>A	ENSP00000506863.1:n.*2544G>A
ENST00000684619.1:c.*2778G>A	ENSP00000508088.1:n.*2778G>A
ENST00000684705.1:n.27G>A
ENST00000684743.1:n.3937G>A
ENST00000260665.12:c.2906G>A MANE Select	ENSP00000260665.7:p.Gly969Asp
ENST00000260665.11:c.2906G>A	ENSP00000260665.7:p.Gly969Asp
NM_133259.3:c.2906G>A	NP_573566.2:p.Gly969Asp
XM_006711915.2:c.2828G>A	XP_006711978.1:p.Gly943Asp
XM_006711916.2:c.2906G>A	XP_006711979.1:p.Gly969Asp
XM_011532473.1:c.2906G>A	XP_011530775.1:p.Gly969Asp
XM_011532474.1:c.2906G>A	XP_011530776.1:p.Gly969Asp
XM_006711916.3:c.2906G>A	XP_006711979.1:p.Gly969Asp
XM_017003117.1:c.2828G>A	XP_016858606.1:p.Gly943Asp
XR_002958896.1:n.2948G>A
NM_133259.4:c.2906G>A MANE Select	NP_573566.2:p.Gly969Asp