Canonical Allele Identifier: CA769115805

Gene: LRPPRC

Linked Data

• dbSNP Id: rs1424308334
• gnomAD v3: 2-43918428-CAATA-C
• gnomAD v4: 2-43918428-CAATA-C
• MyVariant Identifiers: chr2:g.44145568_44145571del (hg19) ; chr2:g.43918429_43918432del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43918433_43918436del , CM000664.2:g.43918433_43918436del	GRCh38
NC_000002.11:g.44145572_44145575del , CM000664.1:g.44145572_44145575del	GRCh37
NC_000002.10:g.43999076_43999079del	NCBI36
NG_008247.1:g.82574_82577del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.415_418del
ENST00000682295.1:c.161-34_161-31del	ENSP00000507499.1:n.161-34_161-31del
ENST00000682303.1:c.*2683-34_*2683-31del	ENSP00000508325.1:n.*2683-34_*2683-31del
ENST00000682308.1:c.2897-34_2897-31del	ENSP00000507056.1:n.2897-34_2897-31del
ENST00000682480.1:c.2897-34_2897-31del	ENSP00000508344.1:n.2897-34_2897-31del
ENST00000682546.1:c.2894-34_2894-31del	ENSP00000508188.1:n.2894-34_2894-31del
ENST00000682585.1:c.2897-34_2897-31del	ENSP00000506885.1:n.2897-34_2897-31del
ENST00000682595.1:n.3481-34_3481-31del
ENST00000682607.1:c.1315-34_1315-31del
ENST00000682779.1:c.2888-34_2888-31del	ENSP00000507947.1:n.2888-34_2888-31del
ENST00000682845.1:n.1999-34_1999-31del
ENST00000682885.1:c.2852-34_2852-31del	ENSP00000508036.1:n.2852-34_2852-31del
ENST00000682933.1:n.2971-34_2971-31del
ENST00000683072.1:n.3481-34_3481-31del
ENST00000683080.1:n.516-34_516-31del
ENST00000683125.1:c.3005-34_3005-31del	ENSP00000507939.1:n.3005-34_3005-31del
ENST00000683213.1:c.2900-34_2900-31del	ENSP00000507751.1:n.2900-34_2900-31del
ENST00000683220.1:c.2927-34_2927-31del	ENSP00000507151.1:n.2927-34_2927-31del
ENST00000683236.1:c.227-34_227-31del	ENSP00000506891.1:n.227-34_227-31del
ENST00000683329.1:n.3700-34_3700-31del
ENST00000683346.1:c.*2772-34_*2772-31del	ENSP00000507458.1:n.*2772-34_*2772-31del
ENST00000683409.1:n.1470_1473del
ENST00000683459.1:n.3484-34_3484-31del
ENST00000683590.1:c.2897-5874_2897-5871del	ENSP00000506820.1:n.2897-5874_2897-5871del
ENST00000683623.1:c.2804-34_2804-31del	ENSP00000507702.1:n.2804-34_2804-31del
ENST00000683645.1:n.3448-34_3448-31del
ENST00000683796.1:c.*2769-34_*2769-31del	ENSP00000508221.1:n.*2769-34_*2769-31del
ENST00000683802.1:n.5822-34_5822-31del
ENST00000683833.1:c.2888-34_2888-31del	ENSP00000506852.1:n.2888-34_2888-31del
ENST00000683994.1:c.2897-34_2897-31del	ENSP00000507181.1:n.2897-34_2897-31del
ENST00000684290.1:c.*433-34_*433-31del	ENSP00000507243.1:n.*433-34_*433-31del
ENST00000684306.1:c.*2810-34_*2810-31del	ENSP00000508384.1:n.*2810-34_*2810-31del
ENST00000684341.1:n.2917-34_2917-31del
ENST00000684383.1:c.*2535-34_*2535-31del	ENSP00000506863.1:n.*2535-34_*2535-31del
ENST00000684619.1:c.*2769-34_*2769-31del	ENSP00000508088.1:n.*2769-34_*2769-31del
ENST00000684743.1:n.3928-34_3928-31del
ENST00000260665.12:c.2897-34_2897-31del MANE Select	ENSP00000260665.7:n.2897-34_2897-31del
ENST00000260665.11:c.2897-34_2897-31del	ENSP00000260665.7:n.2897-34_2897-31del
NM_133259.3:c.2897-34_2897-31del	NP_573566.2:n.2897-34_2897-31del
XM_006711915.2:c.2819-34_2819-31del	XP_006711978.1:n.2819-34_2819-31del
XM_006711916.2:c.2897-34_2897-31del	XP_006711979.1:n.2897-34_2897-31del
XM_011532473.1:c.2897-34_2897-31del	XP_011530775.1:n.2897-34_2897-31del
XM_011532474.1:c.2897-34_2897-31del	XP_011530776.1:n.2897-34_2897-31del
XM_006711916.3:c.2897-34_2897-31del	XP_006711979.1:n.2897-34_2897-31del
XM_017003117.1:c.2819-34_2819-31del	XP_016858606.1:n.2819-34_2819-31del
XR_002958896.1:n.2939-34_2939-31del
NM_133259.4:c.2897-34_2897-31del MANE Select	NP_573566.2:n.2897-34_2897-31del