Canonical Allele Identifier: CA1200472461

Gene: LMNA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156136105_156136106delinsGA , CM000663.2:g.156136105_156136106delinsGA	GRCh38
NC_000001.10:g.156105896_156105897delinsGA , CM000663.1:g.156105896_156105897delinsGA	GRCh37
NC_000001.9:g.154372520_154372521delinsGA	NCBI36
NG_008692.2:g.58533_58534delinsGA , LRG_254:g.58533_58534delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.583_584delinsGA	ENSP00000426535.3:p.Glu195=
ENST00000498722.3:n.373_374delinsGA
ENST00000682650.1:c.1141_1142delinsGA	ENSP00000506904.1:p.Glu381=
ENST00000683032.1:c.1141_1142delinsGA	ENSP00000506771.1:p.Glu381=
ENST00000684195.1:c.1141_1142delinsGA	ENSP00000508220.1:p.Glu381=
ENST00000361308.9:c.1141_1142delinsGA	ENSP00000355292.6:p.Glu381=
ENST00000368300.9:c.1141_1142delinsGA MANE Select	ENSP00000357283.4:p.Glu381=
ENST00000496738.6:n.1516_1517delinsGA
ENST00000674518.1:c.*491_*492delinsGA	ENSP00000502261.1:n.*491_*492delinsGA
ENST00000674600.1:c.*940_*941delinsGA	ENSP00000501666.1:n.*940_*941delinsGA
ENST00000674720.1:c.1141_1142delinsGA	ENSP00000502798.1:p.Glu381=
ENST00000675431.1:n.834_835delinsGA
ENST00000675455.1:c.*941_*942delinsGA	ENSP00000501795.1:n.*941_*942delinsGA
ENST00000675667.1:c.1141_1142delinsGA	ENSP00000501803.1:p.Glu381=
ENST00000675874.1:c.*612_*613delinsGA	ENSP00000501851.1:n.*612_*613delinsGA
ENST00000675881.1:c.*152_*153delinsGA	ENSP00000501670.1:n.*152_*153delinsGA
ENST00000675939.1:c.1141_1142delinsGA	ENSP00000502256.1:p.Glu381=
ENST00000675989.1:n.1516_1517delinsGA
ENST00000676208.1:c.*152_*153delinsGA	ENSP00000502468.1:n.*152_*153delinsGA
ENST00000676283.1:n.1516_1517delinsGA
ENST00000676385.2:c.1141_1142delinsGA	ENSP00000502091.1:p.Glu381=
ENST00000676434.1:c.*152_*153delinsGA	ENSP00000501648.1:n.*152_*153delinsGA
ENST00000677389.1:c.1141_1142delinsGA MANE Plus Clinical	ENSP00000503633.1:p.Glu381=
ENST00000347559.6:c.1141_1142delinsGA	ENSP00000292304.3:p.Glu381=
ENST00000361308.8:c.1141_1142delinsGA	ENSP00000355292.5:p.Glu381=
ENST00000368297.5:c.898_899delinsGA	ENSP00000357280.1:p.Glu300=
ENST00000368298.2:n.405_406delinsGA
ENST00000368299.7:c.1141_1142delinsGA	ENSP00000357282.3:p.Glu381=
ENST00000368300.8:c.1141_1142delinsGA	ENSP00000357283.4:p.Glu381=
ENST00000368301.6:c.1141_1142delinsGA	ENSP00000357284.2:p.Glu381=
ENST00000448611.6:c.805_806delinsGA	ENSP00000395597.2:p.Glu269=
ENST00000473598.6:c.844_845delinsGA	ENSP00000421821.1:p.Glu282=
ENST00000496738.5:n.526_527delinsGA
ENST00000498722.2:n.373_374delinsGA
ENST00000508500.1:c.19_20delinsGA	ENSP00000424977.1:p.Glu7=
NM_001257374.2:c.805_806delinsGA	NP_001244303.1:p.Glu269=
NM_001282624.1:c.898_899delinsGA	NP_001269553.1:p.Glu300=
NM_001282625.1:c.1141_1142delinsGA	NP_001269554.1:p.Glu381=
NM_001282626.1:c.1141_1142delinsGA	NP_001269555.1:p.Glu381=
NM_005572.3:c.1141_1142delinsGA , LRG_254t1:c.1141_1142delinsGA	NP_005563.1:p.Glu381=
NM_170707.3:c.1141_1142delinsGA	NP_733821.1:p.Glu381=
NM_170708.3:c.1141_1142delinsGA	NP_733822.1:p.Glu381=
XM_011509533.1:c.805_806delinsGA	XP_011507835.1:p.Glu269=
XM_011509534.1:c.517_518delinsGA	XP_011507836.1:p.Glu173=
XR_921781.1:n.1430_1431delinsGA
XM_011509534.2:c.517_518delinsGA	XP_011507836.1:p.Glu173=
XR_921781.2:n.1428_1429delinsGA
NM_170707.4:c.1141_1142delinsGA MANE Select	NP_733821.1:p.Glu381=
NM_001257374.3:c.805_806delinsGA	NP_001244303.1:p.Glu269=
NM_001282626.2:c.1141_1142delinsGA	NP_001269555.1:p.Glu381=
NM_001282624.2:c.898_899delinsGA	NP_001269553.1:p.Glu300=
NM_001282625.2:c.1141_1142delinsGA	NP_001269554.1:p.Glu381=
NM_005572.4:c.1141_1142delinsGA MANE Plus Clinical	NP_005563.1:p.Glu381=
NM_170708.4:c.1141_1142delinsGA	NP_733822.1:p.Glu381=