Canonical Allele Identifier: CA1200472879

Gene: LMNA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156137119_156137120delinsGC , CM000663.2:g.156137119_156137120delinsGC	GRCh38
NC_000001.10:g.156106910_156106911delinsGC , CM000663.1:g.156106910_156106911delinsGC	GRCh37
NC_000001.9:g.154373534_154373535delinsGC	NCBI36
NG_008692.2:g.59547_59548delinsGC , LRG_254:g.59547_59548delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000504687.7:c.937_938delinsGC	ENSP00000426535.3:p.Ala313=
ENST00000459904.2:n.743_744delinsGC
ENST00000498722.3:n.727_728delinsGC
ENST00000682650.1:c.1495_1496delinsGC	ENSP00000506904.1:p.Ala499=
ENST00000683032.1:c.1495_1496delinsGC	ENSP00000506771.1:p.Ala499=
ENST00000684195.1:c.1495_1496delinsGC	ENSP00000508220.1:p.Ala499=
ENST00000361308.9:c.1495_1496delinsGC	ENSP00000355292.6:p.Ala499=
ENST00000368300.9:c.1495_1496delinsGC MANE Select	ENSP00000357283.4:p.Ala499=
ENST00000496738.6:n.1954_1955delinsGC
ENST00000674518.1:c.*845_*846delinsGC	ENSP00000502261.1:n.*845_*846delinsGC
ENST00000674600.1:c.*1294_*1295delinsGC	ENSP00000501666.1:n.*1294_*1295delinsGC
ENST00000674720.1:c.*57_*58delinsGC	ENSP00000502798.1:n.*57_*58delinsGC
ENST00000675431.1:n.1188_1189delinsGC
ENST00000675455.1:c.*1295_*1296delinsGC	ENSP00000501795.1:n.*1295_*1296delinsGC
ENST00000675667.1:c.1495_1496delinsGC	ENSP00000501803.1:p.Ala499=
ENST00000675874.1:c.*966_*967delinsGC	ENSP00000501851.1:n.*966_*967delinsGC
ENST00000675881.1:c.*506_*507delinsGC	ENSP00000501670.1:n.*506_*507delinsGC
ENST00000675939.1:c.1495_1496delinsGC	ENSP00000502256.1:p.Ala499=
ENST00000675989.1:n.2354_2355delinsGC
ENST00000676208.1:c.*598_*599delinsGC	ENSP00000502468.1:n.*598_*599delinsGC
ENST00000676283.1:n.1870_1871delinsGC
ENST00000676385.2:c.1495_1496delinsGC	ENSP00000502091.1:p.Ala499=
ENST00000676434.1:c.*506_*507delinsGC	ENSP00000501648.1:n.*506_*507delinsGC
ENST00000677389.1:c.1495_1496delinsGC MANE Plus Clinical	ENSP00000503633.1:p.Ala499=
ENST00000347559.6:c.1495_1496delinsGC	ENSP00000292304.3:p.Ala499=
ENST00000361308.8:c.1312-72_1312-71delinsGC	ENSP00000355292.5:n.1312-72_1312-71delins...
ENST00000368297.5:c.1252_1253delinsGC	ENSP00000357280.1:p.Ala418=
ENST00000368298.2:n.1327_1328delinsGC
ENST00000368299.7:c.1495_1496delinsGC	ENSP00000357282.3:p.Ala499=
ENST00000368300.8:c.1495_1496delinsGC	ENSP00000357283.4:p.Ala499=
ENST00000368301.6:c.1495_1496delinsGC	ENSP00000357284.2:p.Ala499=
ENST00000448611.6:c.1159_1160delinsGC	ENSP00000395597.2:p.Ala387=
ENST00000459904.1:n.743_744delinsGC
ENST00000473598.6:c.1198_1199delinsGC	ENSP00000421821.1:p.Ala400=
ENST00000496738.5:n.964_965delinsGC
ENST00000498722.2:n.727_728delinsGC
ENST00000508500.1:c.373_374delinsGC	ENSP00000424977.1:p.Ala125=
NM_001257374.2:c.1159_1160delinsGC	NP_001244303.1:p.Ala387=
NM_001282624.1:c.1252_1253delinsGC	NP_001269553.1:p.Ala418=
NM_001282625.1:c.1495_1496delinsGC	NP_001269554.1:p.Ala499=
NM_001282626.1:c.1495_1496delinsGC	NP_001269555.1:p.Ala499=
NM_005572.3:c.1495_1496delinsGC , LRG_254t1:c.1495_1496delinsGC	NP_005563.1:p.Ala499=
NM_170707.3:c.1495_1496delinsGC	NP_733821.1:p.Ala499=
NM_170708.3:c.1495_1496delinsGC	NP_733822.1:p.Ala499=
XM_011509533.1:c.1159_1160delinsGC	XP_011507835.1:p.Ala387=
XM_011509534.1:c.871_872delinsGC	XP_011507836.1:p.Ala291=
XR_921781.1:n.1784_1785delinsGC
XM_011509534.2:c.871_872delinsGC	XP_011507836.1:p.Ala291=
XR_921781.2:n.1782_1783delinsGC
NM_170707.4:c.1495_1496delinsGC MANE Select	NP_733821.1:p.Ala499=
NM_001257374.3:c.1159_1160delinsGC	NP_001244303.1:p.Ala387=
NM_001282626.2:c.1495_1496delinsGC	NP_001269555.1:p.Ala499=
NM_001282624.2:c.1252_1253delinsGC	NP_001269553.1:p.Ala418=
NM_001282625.2:c.1495_1496delinsGC	NP_001269554.1:p.Ala499=
NM_005572.4:c.1495_1496delinsGC MANE Plus Clinical	NP_005563.1:p.Ala499=
NM_170708.4:c.1495_1496delinsGC	NP_733822.1:p.Ala499=