Canonical Allele Identifier: CA1143538321

Gene: LMNA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156134477_156134485delinsGCTGCAGAC , CM000663.2:g.156134477_156134485delinsGCTGCAGAC	GRCh38
NC_000001.10:g.156104268_156104276delinsGCTGCAGAC , CM000663.1:g.156104268_156104276delinsGCTGCAGAC	GRCh37
NC_000001.9:g.154370892_154370900delinsGCTGCAGAC	NCBI36
NG_008692.2:g.56905_56913delinsGCTGCAGAC , LRG_254:g.56905_56913delinsGCTGCAGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.30_38delinsGCTGCAGAC	ENSP00000426535.3:p.Arg10=
ENST00000682650.1:c.588_596delinsGCTGCAGAC	ENSP00000506904.1:p.Arg196=
ENST00000683032.1:c.588_596delinsGCTGCAGAC	ENSP00000506771.1:p.Arg196=
ENST00000684195.1:c.588_596delinsGCTGCAGAC	ENSP00000508220.1:p.Arg196=
ENST00000361308.9:c.588_596delinsGCTGCAGAC	ENSP00000355292.6:p.Arg196=
ENST00000368300.9:c.588_596delinsGCTGCAGAC MANE Select	ENSP00000357283.4:p.Arg196=
ENST00000496738.6:n.963_971delinsGCTGCAGAC
ENST00000504687.6:c.-77_-69delinsGCTGCAGAC	ENSP00000426535.2:n.-77_-69delinsGCTGCAGAC
ENST00000674518.1:c.588_596delinsGCTGCAGAC	ENSP00000502261.1:p.Arg196=
ENST00000674600.1:c.*387_*395delinsGCTGCAGAC	ENSP00000501666.1:n.*387_*395delinsGCTGCAGAC
ENST00000674720.1:c.588_596delinsGCTGCAGAC	ENSP00000502798.1:p.Arg196=
ENST00000675431.1:n.281_289delinsGCTGCAGAC
ENST00000675455.1:c.*388_*396delinsGCTGCAGAC	ENSP00000501795.1:n.*388_*396delinsGCTGCAGAC
ENST00000675667.1:c.588_596delinsGCTGCAGAC	ENSP00000501803.1:p.Arg196=
ENST00000675874.1:c.*59_*67delinsGCTGCAGAC	ENSP00000501851.1:n.*59_*67delinsGCTGCAGAC
ENST00000675881.1:c.588_596delinsGCTGCAGAC	ENSP00000501670.1:p.Arg196=
ENST00000675939.1:c.588_596delinsGCTGCAGAC	ENSP00000502256.1:p.Arg196=
ENST00000675989.1:n.963_971delinsGCTGCAGAC
ENST00000676208.1:c.588_596delinsGCTGCAGAC	ENSP00000502468.1:p.Arg196=
ENST00000676283.1:n.963_971delinsGCTGCAGAC
ENST00000676385.2:c.588_596delinsGCTGCAGAC	ENSP00000502091.1:p.Arg196=
ENST00000676434.1:c.588_596delinsGCTGCAGAC	ENSP00000501648.1:p.Arg196=
ENST00000677389.1:c.588_596delinsGCTGCAGAC MANE Plus Clinical	ENSP00000503633.1:p.Arg196=
ENST00000347559.6:c.588_596delinsGCTGCAGAC	ENSP00000292304.3:p.Arg196=
ENST00000361308.8:c.588_596delinsGCTGCAGAC	ENSP00000355292.5:p.Arg196=
ENST00000368297.5:c.345_353delinsGCTGCAGAC	ENSP00000357280.1:p.Arg115=
ENST00000368299.7:c.588_596delinsGCTGCAGAC	ENSP00000357282.3:p.Arg196=
ENST00000368300.8:c.588_596delinsGCTGCAGAC	ENSP00000357283.4:p.Arg196=
ENST00000368301.6:c.588_596delinsGCTGCAGAC	ENSP00000357284.2:p.Arg196=
ENST00000448611.6:c.252_260delinsGCTGCAGAC	ENSP00000395597.2:p.Arg84=
ENST00000470199.2:n.530_538delinsGCTGCAGAC
ENST00000473598.6:c.291_299delinsGCTGCAGAC	ENSP00000421821.1:p.Arg97=
ENST00000502357.5:n.486_494delinsGCTGCAGAC
ENST00000502751.5:n.560_568delinsGCTGCAGAC
ENST00000504687.5:c.339_347delinsGCTGCAGAC	ENSP00000426535.1:p.Arg113=
ENST00000515459.5:c.*262_*270delinsGCTGCAGAC	ENSP00000424518.1:n.*262_*270delinsGCTGCAGAC
NM_001257374.2:c.252_260delinsGCTGCAGAC	NP_001244303.1:p.Arg84=
NM_001282624.1:c.345_353delinsGCTGCAGAC	NP_001269553.1:p.Arg115=
NM_001282625.1:c.588_596delinsGCTGCAGAC	NP_001269554.1:p.Arg196=
NM_001282626.1:c.588_596delinsGCTGCAGAC	NP_001269555.1:p.Arg196=
NM_005572.3:c.588_596delinsGCTGCAGAC , LRG_254t1:c.588_596delinsGCTGCAGAC	NP_005563.1:p.Arg196=
NM_170707.3:c.588_596delinsGCTGCAGAC	NP_733821.1:p.Arg196=
NM_170708.3:c.588_596delinsGCTGCAGAC	NP_733822.1:p.Arg196=
XM_011509533.1:c.252_260delinsGCTGCAGAC	XP_011507835.1:p.Arg84=
XM_011509534.1:c.-77_-69delinsGCTGCAGAC	XP_011507836.1:n.-77_-69delinsGCTGCAGAC
XR_921781.1:n.837_845delinsGCTGCAGAC
XM_011509534.2:c.-77_-69delinsGCTGCAGAC	XP_011507836.1:n.-77_-69delinsGCTGCAGAC
XR_921781.2:n.835_843delinsGCTGCAGAC
NM_170707.4:c.588_596delinsGCTGCAGAC MANE Select	NP_733821.1:p.Arg196=
NM_001257374.3:c.252_260delinsGCTGCAGAC	NP_001244303.1:p.Arg84=
NM_001282626.2:c.588_596delinsGCTGCAGAC	NP_001269555.1:p.Arg196=
NM_001282624.2:c.345_353delinsGCTGCAGAC	NP_001269553.1:p.Arg115=
NM_001282625.2:c.588_596delinsGCTGCAGAC	NP_001269554.1:p.Arg196=
NM_005572.4:c.588_596delinsGCTGCAGAC MANE Plus Clinical	NP_005563.1:p.Arg196=
NM_170708.4:c.588_596delinsGCTGCAGAC	NP_733822.1:p.Arg196=