Canonical Allele Identifier: CA2586964195

Gene: LMNA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156134411_156134425del , CM000663.2:g.156134411_156134425del	GRCh38
NC_000001.10:g.156104202_156104216del , CM000663.1:g.156104202_156104216del	GRCh37
NC_000001.9:g.154370826_154370840del	NCBI36
NG_008692.2:g.56839_56853del , LRG_254:g.56839_56853del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.-37_-23del	ENSP00000426535.3:n.-37_-23del
ENST00000682650.1:c.522_536del	ENSP00000506904.1:p.Ala175_Ala179del
ENST00000683032.1:c.522_536del	ENSP00000506771.1:p.Ala175_Ala179del
ENST00000684195.1:c.522_536del	ENSP00000508220.1:p.Ala175_Ala179del
ENST00000361308.9:c.522_536del	ENSP00000355292.6:p.Ala175_Ala179del
ENST00000368300.9:c.522_536del MANE Select	ENSP00000357283.4:p.Ala175_Ala179del
ENST00000496738.6:n.897_911del
ENST00000504687.6:c.-143_-129del	ENSP00000426535.2:n.-143_-129del
ENST00000674518.1:c.522_536del	ENSP00000502261.1:p.Ala175_Ala179del
ENST00000674600.1:c.*321_*335del	ENSP00000501666.1:n.*321_*335del
ENST00000674720.1:c.522_536del	ENSP00000502798.1:p.Ala175_Ala179del
ENST00000675431.1:n.215_229del
ENST00000675455.1:c.*322_*336del	ENSP00000501795.1:n.*322_*336del
ENST00000675667.1:c.522_536del	ENSP00000501803.1:p.Ala175_Ala179del
ENST00000675874.1:c.365_*7del	ENSP00000501851.1:n.[c.365_*7del;Gln122ProfsTer22]
ENST00000675881.1:c.522_536del	ENSP00000501670.1:p.Ala175_Ala179del
ENST00000675939.1:c.522_536del	ENSP00000502256.1:p.Ala175_Ala179del
ENST00000675989.1:n.897_911del
ENST00000676208.1:c.522_536del	ENSP00000502468.1:p.Ala175_Ala179del
ENST00000676283.1:n.897_911del
ENST00000676385.2:c.522_536del	ENSP00000502091.1:p.Ala175_Ala179del
ENST00000676434.1:c.522_536del	ENSP00000501648.1:p.Ala175_Ala179del
ENST00000677389.1:c.522_536del MANE Plus Clinical	ENSP00000503633.1:p.Ala175_Ala179del
ENST00000347559.6:c.522_536del	ENSP00000292304.3:p.Ala175_Ala179del
ENST00000361308.8:c.522_536del	ENSP00000355292.5:p.Ala175_Ala179del
ENST00000368297.5:c.279_293del	ENSP00000357280.1:p.Ala94_Ala98del
ENST00000368299.7:c.522_536del	ENSP00000357282.3:p.Ala175_Ala179del
ENST00000368300.8:c.522_536del	ENSP00000357283.4:p.Ala175_Ala179del
ENST00000368301.6:c.522_536del	ENSP00000357284.2:p.Ala175_Ala179del
ENST00000448611.6:c.186_200del	ENSP00000395597.2:p.Ala63_Ala67del
ENST00000469565.6:n.556_570del
ENST00000470199.2:n.464_478del
ENST00000473598.6:c.225_239del	ENSP00000421821.1:p.Ala76_Ala80del
ENST00000502357.5:n.420_434del
ENST00000502751.5:n.494_508del
ENST00000504687.5:c.273_287del	ENSP00000426535.1:p.Ala92_Ala96del
ENST00000515459.5:c.*196_*210del	ENSP00000424518.1:n.*196_*210del
NM_001257374.2:c.186_200del	NP_001244303.1:p.Ala63_Ala67del
NM_001282624.1:c.279_293del	NP_001269553.1:p.Ala94_Ala98del
NM_001282625.1:c.522_536del	NP_001269554.1:p.Ala175_Ala179del
NM_001282626.1:c.522_536del	NP_001269555.1:p.Ala175_Ala179del
NM_005572.3:c.522_536del , LRG_254t1:c.522_536del	NP_005563.1:p.Ala175_Ala179del
NM_170707.3:c.522_536del	NP_733821.1:p.Ala175_Ala179del
NM_170708.3:c.522_536del	NP_733822.1:p.Ala175_Ala179del
XM_011509533.1:c.186_200del	XP_011507835.1:p.Ala63_Ala67del
XM_011509534.1:c.-143_-129del	XP_011507836.1:n.-143_-129del
XR_921781.1:n.771_785del
XM_011509534.2:c.-143_-129del	XP_011507836.1:n.-143_-129del
XR_921781.2:n.769_783del
NM_170707.4:c.522_536del MANE Select	NP_733821.1:p.Ala175_Ala179del
NM_001257374.3:c.186_200del	NP_001244303.1:p.Ala63_Ala67del
NM_001282626.2:c.522_536del	NP_001269555.1:p.Ala175_Ala179del
NM_001282624.2:c.279_293del	NP_001269553.1:p.Ala94_Ala98del
NM_001282625.2:c.522_536del	NP_001269554.1:p.Ala175_Ala179del
NM_005572.4:c.522_536del MANE Plus Clinical	NP_005563.1:p.Ala175_Ala179del
NM_170708.4:c.522_536del	NP_733822.1:p.Ala175_Ala179del