Canonical Allele Identifier: CA769115913

Gene: LRPPRC

Linked Data

• dbSNP Id: rs1264310541
• MyVariant Identifiers: chr2:g.44145697del (hg19) ; chr2:g.43918558del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43918560del , CM000664.2:g.43918560del	GRCh38
NC_000002.11:g.44145699del , CM000664.1:g.44145699del	GRCh37
NC_000002.10:g.43999203del	NCBI36
NG_008247.1:g.82448del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.289del
ENST00000682295.1:c.161-160del	ENSP00000507499.1:n.161-160del
ENST00000682303.1:c.*2683-160del	ENSP00000508325.1:n.*2683-160del
ENST00000682308.1:c.2897-160del	ENSP00000507056.1:n.2897-160del
ENST00000682480.1:c.2897-160del	ENSP00000508344.1:n.2897-160del
ENST00000682546.1:c.2894-160del	ENSP00000508188.1:n.2894-160del
ENST00000682585.1:c.2897-160del	ENSP00000506885.1:n.2897-160del
ENST00000682595.1:n.3481-160del
ENST00000682607.1:c.1315-160del
ENST00000682779.1:c.2888-160del	ENSP00000507947.1:n.2888-160del
ENST00000682845.1:n.1999-160del
ENST00000682885.1:c.2852-160del	ENSP00000508036.1:n.2852-160del
ENST00000682933.1:n.2971-160del
ENST00000683072.1:n.3481-160del
ENST00000683080.1:n.516-160del
ENST00000683125.1:c.3005-160del	ENSP00000507939.1:n.3005-160del
ENST00000683213.1:c.2900-160del	ENSP00000507751.1:n.2900-160del
ENST00000683220.1:c.2927-160del	ENSP00000507151.1:n.2927-160del
ENST00000683236.1:c.227-160del	ENSP00000506891.1:n.227-160del
ENST00000683329.1:n.3700-160del
ENST00000683346.1:c.*2772-160del	ENSP00000507458.1:n.*2772-160del
ENST00000683409.1:n.1344del
ENST00000683459.1:n.3484-160del
ENST00000683590.1:c.2897-6000del	ENSP00000506820.1:n.2897-6000del
ENST00000683623.1:c.2804-160del	ENSP00000507702.1:n.2804-160del
ENST00000683645.1:n.3448-160del
ENST00000683796.1:c.*2769-160del	ENSP00000508221.1:n.*2769-160del
ENST00000683802.1:n.5822-160del
ENST00000683833.1:c.2888-160del	ENSP00000506852.1:n.2888-160del
ENST00000683994.1:c.2897-160del	ENSP00000507181.1:n.2897-160del
ENST00000684290.1:c.*433-160del	ENSP00000507243.1:n.*433-160del
ENST00000684306.1:c.*2810-160del	ENSP00000508384.1:n.*2810-160del
ENST00000684341.1:n.2917-160del
ENST00000684383.1:c.*2535-160del	ENSP00000506863.1:n.*2535-160del
ENST00000684619.1:c.*2769-160del	ENSP00000508088.1:n.*2769-160del
ENST00000684743.1:n.3928-160del
ENST00000260665.12:c.2897-160del MANE Select	ENSP00000260665.7:n.2897-160del
ENST00000260665.11:c.2897-160del	ENSP00000260665.7:n.2897-160del
NM_133259.3:c.2897-160del	NP_573566.2:n.2897-160del
XM_006711915.2:c.2819-160del	XP_006711978.1:n.2819-160del
XM_006711916.2:c.2897-160del	XP_006711979.1:n.2897-160del
XM_011532473.1:c.2897-160del	XP_011530775.1:n.2897-160del
XM_011532474.1:c.2897-160del	XP_011530776.1:n.2897-160del
XM_006711916.3:c.2897-160del	XP_006711979.1:n.2897-160del
XM_017003117.1:c.2819-160del	XP_016858606.1:n.2819-160del
XR_002958896.1:n.2939-160del
NM_133259.4:c.2897-160del MANE Select	NP_573566.2:n.2897-160del