Canonical Allele Identifier: CA425908492

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44145213A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43918074A>T , CM000664.2:g.43918074A>T	GRCh38
NC_000002.11:g.44145213A>T , CM000664.1:g.44145213A>T	GRCh37
NC_000002.10:g.43998717A>T	NCBI36
NG_008247.1:g.82932T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.651T>A
ENST00000682295.1:c.303+182T>A	ENSP00000507499.1:n.303+182T>A
ENST00000682303.1:c.*2885T>A	ENSP00000508325.1:n.*2885T>A
ENST00000682308.1:c.3099T>A	ENSP00000507056.1:p.Pro1033=
ENST00000682480.1:c.3117T>A	ENSP00000508344.1:p.Pro1039=
ENST00000682546.1:c.3096T>A	ENSP00000508188.1:p.Pro1032=
ENST00000682585.1:c.3099T>A	ENSP00000506885.1:p.Pro1033=
ENST00000682595.1:n.3683T>A
ENST00000682607.1:c.1517T>A
ENST00000682779.1:c.3090T>A	ENSP00000507947.1:p.Pro1030=
ENST00000682845.1:n.2201T>A
ENST00000682885.1:c.3054T>A	ENSP00000508036.1:p.Pro1018=
ENST00000682933.1:n.3173T>A
ENST00000683072.1:n.3683T>A
ENST00000683080.1:n.718T>A
ENST00000683125.1:c.3207T>A	ENSP00000507939.1:p.Pro1069=
ENST00000683213.1:c.3102T>A	ENSP00000507751.1:p.Pro1034=
ENST00000683220.1:c.3129T>A	ENSP00000507151.1:p.Pro1043=
ENST00000683329.1:n.3902T>A
ENST00000683346.1:c.*2974T>A	ENSP00000507458.1:n.*2974T>A
ENST00000683409.1:n.1706T>A
ENST00000683459.1:n.3686T>A
ENST00000683590.1:c.2897-5516T>A	ENSP00000506820.1:n.2897-5516T>A
ENST00000683623.1:c.3006T>A	ENSP00000507702.1:p.Pro1002=
ENST00000683645.1:n.3650T>A
ENST00000683796.1:c.*2971T>A	ENSP00000508221.1:n.*2971T>A
ENST00000683802.1:n.6024T>A
ENST00000683833.1:c.3090T>A	ENSP00000506852.1:p.Pro1030=
ENST00000683994.1:c.3099T>A	ENSP00000507181.1:p.Pro1033=
ENST00000684290.1:c.*635T>A	ENSP00000507243.1:n.*635T>A
ENST00000684306.1:c.*3012T>A	ENSP00000508384.1:n.*3012T>A
ENST00000684341.1:n.3119T>A
ENST00000684383.1:c.*2737T>A	ENSP00000506863.1:n.*2737T>A
ENST00000684619.1:c.*2971T>A	ENSP00000508088.1:n.*2971T>A
ENST00000684705.1:n.220T>A
ENST00000684743.1:n.4130T>A
ENST00000260665.12:c.3099T>A MANE Select	ENSP00000260665.7:p.Pro1033=
ENST00000260665.11:c.3099T>A	ENSP00000260665.7:p.Pro1033=
NM_133259.3:c.3099T>A	NP_573566.2:p.Pro1033=
XM_006711915.2:c.3021T>A	XP_006711978.1:p.Pro1007=
XM_006711916.2:c.3099T>A	XP_006711979.1:p.Pro1033=
XM_011532473.1:c.3099T>A	XP_011530775.1:p.Pro1033=
XM_011532474.1:c.3099T>A	XP_011530776.1:p.Pro1033=
XM_006711916.3:c.3099T>A	XP_006711979.1:p.Pro1033=
XM_017003117.1:c.3021T>A	XP_016858606.1:p.Pro1007=
XR_002958896.1:n.3141T>A
NM_133259.4:c.3099T>A MANE Select	NP_573566.2:p.Pro1033=