Canonical Allele Identifier: CA2494002735

Gene: LRPPRC

Linked Data

• ClinVar Variation Id: 2992421
• ClinVar RCV Id: RCV003855548
• dbSNP Id: rs1672639850
• gnomAD v4: 2-43945312-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43945315del , CM000664.2:g.43945315del	GRCh38
NC_000002.11:g.44172454del , CM000664.1:g.44172454del	GRCh37
NC_000002.10:g.44025958del	NCBI36
NG_008247.1:g.55693del

Transcript Alleles

HGVS	Amino-acid change
ENST00000409659.6:c.2296+19del	ENSP00000386562.2:n.2296+19del
ENST00000447246.2:c.2296+19del	ENSP00000403637.2:n.2296+19del
ENST00000681961.1:n.2316+19del
ENST00000682104.1:c.2170+19del	ENSP00000507716.1:n.2170+19del
ENST00000682303.1:c.*2082+800del	ENSP00000508325.1:n.*2082+800del
ENST00000682308.1:c.2296+19del	ENSP00000507056.1:n.2296+19del
ENST00000682480.1:c.2296+19del	ENSP00000508344.1:n.2296+19del
ENST00000682546.1:c.2293+19del	ENSP00000508188.1:n.2293+19del
ENST00000682585.1:c.2296+19del	ENSP00000506885.1:n.2296+19del
ENST00000682595.1:n.2878+19del
ENST00000682607.1:c.714+19del
ENST00000682779.1:c.2287+19del	ENSP00000507947.1:n.2287+19del
ENST00000682885.1:c.2251+19del	ENSP00000508036.1:n.2251+19del
ENST00000682933.1:n.2370+19del
ENST00000683072.1:n.2878+19del
ENST00000683125.1:c.2296+19del	ENSP00000507939.1:n.2296+19del
ENST00000683213.1:c.2299+19del	ENSP00000507751.1:n.2299+19del
ENST00000683220.1:c.2326+19del	ENSP00000507151.1:n.2326+19del
ENST00000683329.1:n.3099+19del
ENST00000683346.1:c.*2171+19del	ENSP00000507458.1:n.*2171+19del
ENST00000683459.1:n.2883+19del
ENST00000683590.1:c.2296+19del	ENSP00000506820.1:n.2296+19del
ENST00000683623.1:c.2296+19del	ENSP00000507702.1:n.2296+19del
ENST00000683645.1:n.2847+19del
ENST00000683694.1:n.1047+19del
ENST00000683796.1:c.*2168+19del	ENSP00000508221.1:n.*2168+19del
ENST00000683802.1:n.5221+19del
ENST00000683833.1:c.2287+19del	ENSP00000506852.1:n.2287+19del
ENST00000683989.1:c.2296+19del	ENSP00000507510.1:n.2296+19del
ENST00000683994.1:c.2296+19del	ENSP00000507181.1:n.2296+19del
ENST00000684290.1:c.2210+800del	ENSP00000507243.1:n.2210+800del
ENST00000684306.1:c.*2209+19del	ENSP00000508384.1:n.*2209+19del
ENST00000684341.1:n.2316+19del
ENST00000684383.1:c.*1934+19del	ENSP00000506863.1:n.*1934+19del
ENST00000684619.1:c.*2168+19del	ENSP00000508088.1:n.*2168+19del
ENST00000684743.1:n.3327+19del
ENST00000260665.12:c.2296+19del MANE Select	ENSP00000260665.7:n.2296+19del
ENST00000260665.11:c.2296+19del	ENSP00000260665.7:n.2296+19del
NM_133259.3:c.2296+19del	NP_573566.2:n.2296+19del
XM_006711915.2:c.2218+19del	XP_006711978.1:n.2218+19del
XM_006711916.2:c.2296+19del	XP_006711979.1:n.2296+19del
XM_011532473.1:c.2296+19del	XP_011530775.1:n.2296+19del
XM_011532474.1:c.2296+19del	XP_011530776.1:n.2296+19del
XM_006711916.3:c.2296+19del	XP_006711979.1:n.2296+19del
XM_017003117.1:c.2218+19del	XP_016858606.1:n.2218+19del
XR_002958896.1:n.2338+19del
NM_133259.4:c.2296+19del MANE Select	NP_573566.2:n.2296+19del