Canonical Allele Identifier: CA2586964193

Gene: LMNA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156130756del , CM000663.2:g.156130756del	GRCh38
NC_000001.10:g.156100547del , CM000663.1:g.156100547del	GRCh37
NC_000001.9:g.154367171del	NCBI36
NG_008692.2:g.53184del , LRG_254:g.53184del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.-63del	ENSP00000426535.3:n.-63del
ENST00000682650.1:c.496del	ENSP00000506904.1:p.Arg166GlyfsTer11
ENST00000683032.1:c.496del	ENSP00000506771.1:p.Arg166GlyfsTer11
ENST00000684195.1:c.496del	ENSP00000508220.1:p.Arg166GlyfsTer11
ENST00000361308.9:c.496del	ENSP00000355292.6:p.Arg166GlyfsTer11
ENST00000368300.9:c.496del MANE Select	ENSP00000357283.4:p.Arg166GlyfsTer11
ENST00000496738.6:n.871del
ENST00000504687.6:c.-169del	ENSP00000426535.2:n.-169del
ENST00000674518.1:c.496del	ENSP00000502261.1:p.Arg166GlyfsTer11
ENST00000674600.1:c.*295del	ENSP00000501666.1:n.*295del
ENST00000674720.1:c.496del	ENSP00000502798.1:p.Arg166GlyfsTer11
ENST00000675431.1:n.189del
ENST00000675455.1:c.*296del	ENSP00000501795.1:n.*296del
ENST00000675667.1:c.496del	ENSP00000501803.1:p.Arg166GlyfsTer11
ENST00000675874.1:c.357-3647del	ENSP00000501851.1:n.357-3647del
ENST00000675881.1:c.496del	ENSP00000501670.1:p.Arg166GlyfsTer11
ENST00000675939.1:c.496del	ENSP00000502256.1:p.Arg166GlyfsTer11
ENST00000675989.1:n.871del
ENST00000676208.1:c.496del	ENSP00000502468.1:p.Arg166GlyfsTer11
ENST00000676283.1:n.871del
ENST00000676385.2:c.496del	ENSP00000502091.1:p.Arg166GlyfsTer11
ENST00000676434.1:c.496del	ENSP00000501648.1:p.Arg166GlyfsTer11
ENST00000677389.1:c.496del MANE Plus Clinical	ENSP00000503633.1:p.Arg166GlyfsTer11
ENST00000347559.6:c.496del	ENSP00000292304.3:p.Arg166GlyfsTer11
ENST00000361308.8:c.496del	ENSP00000355292.5:p.Arg166GlyfsTer11
ENST00000368297.5:c.253del	ENSP00000357280.1:p.Arg85GlyfsTer11
ENST00000368299.7:c.496del	ENSP00000357282.3:p.Arg166GlyfsTer11
ENST00000368300.8:c.496del	ENSP00000357283.4:p.Arg166GlyfsTer11
ENST00000368301.6:c.496del	ENSP00000357284.2:p.Arg166GlyfsTer11
ENST00000448611.6:c.160del	ENSP00000395597.2:p.Arg54GlyfsTer11
ENST00000469565.6:n.530del
ENST00000470199.2:n.438del
ENST00000473598.6:c.199del	ENSP00000421821.1:p.Arg67GlyfsTer11
ENST00000502357.5:n.394del
ENST00000502751.5:n.468del
ENST00000504687.5:c.247del	ENSP00000426535.1:p.Arg83GlyfsTer11
ENST00000515459.5:c.*170del	ENSP00000424518.1:n.*170del
NM_001257374.2:c.160del	NP_001244303.1:p.Arg54GlyfsTer11
NM_001282624.1:c.253del	NP_001269553.1:p.Arg85GlyfsTer11
NM_001282625.1:c.496del	NP_001269554.1:p.Arg166GlyfsTer11
NM_001282626.1:c.496del	NP_001269555.1:p.Arg166GlyfsTer11
NM_005572.3:c.496del , LRG_254t1:c.496del	NP_005563.1:p.Arg166GlyfsTer11
NM_170707.3:c.496del	NP_733821.1:p.Arg166GlyfsTer11
NM_170708.3:c.496del	NP_733822.1:p.Arg166GlyfsTer11
XM_011509533.1:c.160del	XP_011507835.1:p.Arg54GlyfsTer11
XM_011509534.1:c.-169del	XP_011507836.1:n.-169del
XR_921781.1:n.745del
XM_011509534.2:c.-169del	XP_011507836.1:n.-169del
XR_921781.2:n.743del
NM_170707.4:c.496del MANE Select	NP_733821.1:p.Arg166GlyfsTer11
NM_001257374.3:c.160del	NP_001244303.1:p.Arg54GlyfsTer11
NM_001282626.2:c.496del	NP_001269555.1:p.Arg166GlyfsTer11
NM_001282624.2:c.253del	NP_001269553.1:p.Arg85GlyfsTer11
NM_001282625.2:c.496del	NP_001269554.1:p.Arg166GlyfsTer11
NM_005572.4:c.496del MANE Plus Clinical	NP_005563.1:p.Arg166GlyfsTer11
NM_170708.4:c.496del	NP_733822.1:p.Arg166GlyfsTer11