Canonical Allele Identifier: CA1200472399

Gene: LMNA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156135946_156135960delinsGCCCGTGAGCGGGAC , CM000663.2:g.156135946_156135960delinsGCCCGTGAGCGGGAC	GRCh38
NC_000001.10:g.156105737_156105751delinsGCCCGTGAGCGGGAC , CM000663.1:g.156105737_156105751delinsGCCCGTGAGCGGGAC	GRCh37
NC_000001.9:g.154372361_154372375delinsGCCCGTGAGCGGGAC	NCBI36
NG_008692.2:g.58374_58388delinsGCCCGTGAGCGGGAC , LRG_254:g.58374_58388delinsGCCCGTGAGCGGGAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000504687.7:c.424_438delinsGCCCGTGAGCGGGAC	ENSP00000426535.3:p.Ala142=
ENST00000498722.3:n.214_228delinsGCCCGTGAGCGGGAC
ENST00000682650.1:c.982_996delinsGCCCGTGAGCGGGAC	ENSP00000506904.1:p.Ala328=
ENST00000683032.1:c.982_996delinsGCCCGTGAGCGGGAC	ENSP00000506771.1:p.Ala328=
ENST00000684195.1:c.982_996delinsGCCCGTGAGCGGGAC	ENSP00000508220.1:p.Ala328=
ENST00000361308.9:c.982_996delinsGCCCGTGAGCGGGAC	ENSP00000355292.6:p.Ala328=
ENST00000368300.9:c.982_996delinsGCCCGTGAGCGGGAC MANE Select	ENSP00000357283.4:p.Ala328=
ENST00000496738.6:n.1357_1371delinsGCCCGTGAGCGGGAC
ENST00000674518.1:c.*332_*346delinsGCCCGTGAGCGGGAC	ENSP00000502261.1:n.*332_*346delinsGCCCGTGAGCGGGAC
ENST00000674600.1:c.*781_*795delinsGCCCGTGAGCGGGAC	ENSP00000501666.1:n.*781_*795delinsGCCCGTGAGCGGGAC
ENST00000674720.1:c.982_996delinsGCCCGTGAGCGGGAC	ENSP00000502798.1:p.Ala328=
ENST00000675431.1:n.675_689delinsGCCCGTGAGCGGGAC
ENST00000675455.1:c.*782_*796delinsGCCCGTGAGCGGGAC	ENSP00000501795.1:n.*782_*796delinsGCCCGTGAGCGGGAC
ENST00000675667.1:c.982_996delinsGCCCGTGAGCGGGAC	ENSP00000501803.1:p.Ala328=
ENST00000675874.1:c.*453_*467delinsGCCCGTGAGCGGGAC	ENSP00000501851.1:n.*453_*467delinsGCCCGTGAGCGGGAC
ENST00000675881.1:c.1022_*7delinsGCCCGTGAGCGGGAC	ENSP00000501670.1:n.[c.1022_*7delinsGCCCGTGAGCGGGAC;Gly341=]
ENST00000675939.1:c.982_996delinsGCCCGTGAGCGGGAC	ENSP00000502256.1:p.Ala328=
ENST00000675989.1:n.1357_1371delinsGCCCGTGAGCGGGAC
ENST00000676208.1:c.1022_*7delinsGCCCGTGAGCGGGAC	ENSP00000502468.1:n.[c.1022_*7delinsGCCCGTGAGCGGGAC;Gly341=]
ENST00000676283.1:n.1357_1371delinsGCCCGTGAGCGGGAC
ENST00000676385.2:c.982_996delinsGCCCGTGAGCGGGAC	ENSP00000502091.1:p.Ala328=
ENST00000676434.1:c.1022_*7delinsGCCCGTGAGCGGGAC	ENSP00000501648.1:n.[c.1022_*7delinsGCCCGTGAGCGGGAC;Gly341=]
ENST00000677389.1:c.982_996delinsGCCCGTGAGCGGGAC MANE Plus Clinical	ENSP00000503633.1:p.Ala328=
ENST00000347559.6:c.982_996delinsGCCCGTGAGCGGGAC	ENSP00000292304.3:p.Ala328=
ENST00000361308.8:c.982_996delinsGCCCGTGAGCGGGAC	ENSP00000355292.5:p.Ala328=
ENST00000368297.5:c.739_753delinsGCCCGTGAGCGGGAC	ENSP00000357280.1:p.Ala247=
ENST00000368298.2:n.246_260delinsGCCCGTGAGCGGGAC
ENST00000368299.7:c.982_996delinsGCCCGTGAGCGGGAC	ENSP00000357282.3:p.Ala328=
ENST00000368300.8:c.982_996delinsGCCCGTGAGCGGGAC	ENSP00000357283.4:p.Ala328=
ENST00000368301.6:c.982_996delinsGCCCGTGAGCGGGAC	ENSP00000357284.2:p.Ala328=
ENST00000448611.6:c.646_660delinsGCCCGTGAGCGGGAC	ENSP00000395597.2:p.Ala216=
ENST00000473598.6:c.685_699delinsGCCCGTGAGCGGGAC	ENSP00000421821.1:p.Ala229=
ENST00000496738.5:n.367_381delinsGCCCGTGAGCGGGAC
ENST00000498722.2:n.214_228delinsGCCCGTGAGCGGGAC
NM_001257374.2:c.646_660delinsGCCCGTGAGCGGGAC	NP_001244303.1:p.Ala216=
NM_001282624.1:c.739_753delinsGCCCGTGAGCGGGAC	NP_001269553.1:p.Ala247=
NM_001282625.1:c.982_996delinsGCCCGTGAGCGGGAC	NP_001269554.1:p.Ala328=
NM_001282626.1:c.982_996delinsGCCCGTGAGCGGGAC	NP_001269555.1:p.Ala328=
NM_005572.3:c.982_996delinsGCCCGTGAGCGGGAC , LRG_254t1:c.982_996delinsGCCCGTGAGCGGGAC	NP_005563.1:p.Ala328=
NM_170707.3:c.982_996delinsGCCCGTGAGCGGGAC	NP_733821.1:p.Ala328=
NM_170708.3:c.982_996delinsGCCCGTGAGCGGGAC	NP_733822.1:p.Ala328=
XM_011509533.1:c.646_660delinsGCCCGTGAGCGGGAC	XP_011507835.1:p.Ala216=
XM_011509534.1:c.358_372delinsGCCCGTGAGCGGGAC	XP_011507836.1:p.Ala120=
XR_921781.1:n.1271_1285delinsGCCCGTGAGCGGGAC
XM_011509534.2:c.358_372delinsGCCCGTGAGCGGGAC	XP_011507836.1:p.Ala120=
XR_921781.2:n.1269_1283delinsGCCCGTGAGCGGGAC
NM_170707.4:c.982_996delinsGCCCGTGAGCGGGAC MANE Select	NP_733821.1:p.Ala328=
NM_001257374.3:c.646_660delinsGCCCGTGAGCGGGAC	NP_001244303.1:p.Ala216=
NM_001282626.2:c.982_996delinsGCCCGTGAGCGGGAC	NP_001269555.1:p.Ala328=
NM_001282624.2:c.739_753delinsGCCCGTGAGCGGGAC	NP_001269553.1:p.Ala247=
NM_001282625.2:c.982_996delinsGCCCGTGAGCGGGAC	NP_001269554.1:p.Ala328=
NM_005572.4:c.982_996delinsGCCCGTGAGCGGGAC MANE Plus Clinical	NP_005563.1:p.Ala328=
NM_170708.4:c.982_996delinsGCCCGTGAGCGGGAC	NP_733822.1:p.Ala328=