Canonical Allele Identifier: CA769069303

Gene: LRPPRC

Linked Data

• dbSNP Id: rs1242827636
• MyVariant Identifiers: chr2:g.44175143_44175153del (hg19) ; chr2:g.43948004_43948014del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43948004_43948014del , CM000664.2:g.43948004_43948014del	GRCh38
NC_000002.11:g.44175143_44175153del , CM000664.1:g.44175143_44175153del	GRCh37
NC_000002.10:g.44028647_44028657del	NCBI36
NG_008247.1:g.52992_53002del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409659.6:c.1920+108_1920+118del	ENSP00000386562.2:n.1920+108_1920+118del
ENST00000447246.2:c.1920+108_1920+118del	ENSP00000403637.2:n.1920+108_1920+118del
ENST00000681959.1:n.1534+108_1534+118del
ENST00000681961.1:n.1940+108_1940+118del
ENST00000682104.1:c.1794+108_1794+118del	ENSP00000507716.1:n.1794+108_1794+118del
ENST00000682303.1:c.*1792+108_*1792+118del	ENSP00000508325.1:n.*1792+108_*1792+118del
ENST00000682308.1:c.1920+108_1920+118del	ENSP00000507056.1:n.1920+108_1920+118del
ENST00000682480.1:c.1920+108_1920+118del	ENSP00000508344.1:n.1920+108_1920+118del
ENST00000682546.1:c.1917+108_1917+118del	ENSP00000508188.1:n.1917+108_1917+118del
ENST00000682585.1:c.1920+108_1920+118del	ENSP00000506885.1:n.1920+108_1920+118del
ENST00000682595.1:n.2502+108_2502+118del
ENST00000682607.1:c.338+108_338+118del
ENST00000682779.1:c.1911+108_1911+118del	ENSP00000507947.1:n.1911+108_1911+118del
ENST00000682885.1:c.1920+108_1920+118del	ENSP00000508036.1:n.1920+108_1920+118del
ENST00000682933.1:n.1994+108_1994+118del
ENST00000683072.1:n.2502+108_2502+118del
ENST00000683082.1:n.2046_2056del
ENST00000683125.1:c.1920+108_1920+118del	ENSP00000507939.1:n.1920+108_1920+118del
ENST00000683213.1:c.1923+108_1923+118del	ENSP00000507751.1:n.1923+108_1923+118del
ENST00000683220.1:c.1950+108_1950+118del	ENSP00000507151.1:n.1950+108_1950+118del
ENST00000683329.1:n.2723+108_2723+118del
ENST00000683346.1:c.*1795+108_*1795+118del	ENSP00000507458.1:n.*1795+108_*1795+118del
ENST00000683459.1:n.2507+108_2507+118del
ENST00000683590.1:c.1920+108_1920+118del	ENSP00000506820.1:n.1920+108_1920+118del
ENST00000683623.1:c.1920+108_1920+118del	ENSP00000507702.1:n.1920+108_1920+118del
ENST00000683645.1:n.2471+108_2471+118del
ENST00000683694.1:n.671+108_671+118del
ENST00000683796.1:c.*1792+108_*1792+118del	ENSP00000508221.1:n.*1792+108_*1792+118del
ENST00000683802.1:n.4845+108_4845+118del
ENST00000683833.1:c.1911+108_1911+118del	ENSP00000506852.1:n.1911+108_1911+118del
ENST00000683934.1:c.1806+108_1806+118del
ENST00000683989.1:c.1920+108_1920+118del	ENSP00000507510.1:n.1920+108_1920+118del
ENST00000683994.1:c.1920+108_1920+118del	ENSP00000507181.1:n.1920+108_1920+118del
ENST00000684290.1:c.1920+108_1920+118del	ENSP00000507243.1:n.1920+108_1920+118del
ENST00000684306.1:c.*1833+108_*1833+118del	ENSP00000508384.1:n.*1833+108_*1833+118del
ENST00000684341.1:n.1940+108_1940+118del
ENST00000684383.1:c.*1558+108_*1558+118del	ENSP00000506863.1:n.*1558+108_*1558+118del
ENST00000684482.1:c.4389+108_4389+118del
ENST00000684619.1:c.*1792+108_*1792+118del	ENSP00000508088.1:n.*1792+108_*1792+118del
ENST00000684743.1:n.2951+108_2951+118del
ENST00000260665.12:c.1920+108_1920+118del MANE Select	ENSP00000260665.7:n.1920+108_1920+118del
ENST00000260665.11:c.1920+108_1920+118del	ENSP00000260665.7:n.1920+108_1920+118del
NM_133259.3:c.1920+108_1920+118del	NP_573566.2:n.1920+108_1920+118del
XM_006711915.2:c.1842+108_1842+118del	XP_006711978.1:n.1842+108_1842+118del
XM_006711916.2:c.1920+108_1920+118del	XP_006711979.1:n.1920+108_1920+118del
XM_011532473.1:c.1920+108_1920+118del	XP_011530775.1:n.1920+108_1920+118del
XM_011532474.1:c.1920+108_1920+118del	XP_011530776.1:n.1920+108_1920+118del
XM_006711916.3:c.1920+108_1920+118del	XP_006711979.1:n.1920+108_1920+118del
XM_017003117.1:c.1842+108_1842+118del	XP_016858606.1:n.1842+108_1842+118del
XR_002958896.1:n.1962+108_1962+118del
NM_133259.4:c.1920+108_1920+118del MANE Select	NP_573566.2:n.1920+108_1920+118del