Canonical Allele Identifier: CA2574066319

Gene: LMNA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156136149_156136151del , CM000663.2:g.156136149_156136151del	GRCh38
NC_000001.10:g.156105940_156105942del , CM000663.1:g.156105940_156105942del	GRCh37
NC_000001.9:g.154372564_154372566del	NCBI36
NG_008692.2:g.58577_58579del , LRG_254:g.58577_58579del

Transcript Alleles

HGVS	Amino-acid change
ENST00000504687.7:c.599+28_599+30del	ENSP00000426535.3:n.599+28_599+30del
ENST00000498722.3:n.389+28_389+30del
ENST00000682650.1:c.1157+28_1157+30del	ENSP00000506904.1:n.1157+28_1157+30del
ENST00000683032.1:c.1157+28_1157+30del	ENSP00000506771.1:n.1157+28_1157+30del
ENST00000684195.1:c.1157+28_1157+30del	ENSP00000508220.1:n.1157+28_1157+30del
ENST00000361308.9:c.1157+28_1157+30del	ENSP00000355292.6:n.1157+28_1157+30del
ENST00000368300.9:c.1157+28_1157+30del MANE Select	ENSP00000357283.4:n.1157+28_1157+30del
ENST00000496738.6:n.1532+28_1532+30del
ENST00000674518.1:c.*507+28_*507+30del	ENSP00000502261.1:n.*507+28_*507+30del
ENST00000674600.1:c.*956+28_*956+30del	ENSP00000501666.1:n.*956+28_*956+30del
ENST00000674720.1:c.1157+28_1157+30del	ENSP00000502798.1:n.1157+28_1157+30del
ENST00000675431.1:n.850+28_850+30del
ENST00000675455.1:c.*957+28_*957+30del	ENSP00000501795.1:n.*957+28_*957+30del
ENST00000675667.1:c.1157+28_1157+30del	ENSP00000501803.1:n.1157+28_1157+30del
ENST00000675874.1:c.*628+28_*628+30del	ENSP00000501851.1:n.*628+28_*628+30del
ENST00000675881.1:c.*168+28_*168+30del	ENSP00000501670.1:n.*168+28_*168+30del
ENST00000675939.1:c.1157+28_1157+30del	ENSP00000502256.1:n.1157+28_1157+30del
ENST00000675989.1:n.1532+28_1532+30del
ENST00000676208.1:c.*196_*198del	ENSP00000502468.1:n.*196_*198del
ENST00000676283.1:n.1532+28_1532+30del
ENST00000676385.2:c.1157+28_1157+30del	ENSP00000502091.1:n.1157+28_1157+30del
ENST00000676434.1:c.*168+28_*168+30del	ENSP00000501648.1:n.*168+28_*168+30del
ENST00000677389.1:c.1157+28_1157+30del MANE Plus Clinical	ENSP00000503633.1:n.1157+28_1157+30del
ENST00000347559.6:c.1157+28_1157+30del	ENSP00000292304.3:n.1157+28_1157+30del
ENST00000361308.8:c.1157+28_1157+30del	ENSP00000355292.5:n.1157+28_1157+30del
ENST00000368297.5:c.914+28_914+30del	ENSP00000357280.1:n.914+28_914+30del
ENST00000368298.2:n.421+28_421+30del
ENST00000368299.7:c.1157+28_1157+30del	ENSP00000357282.3:n.1157+28_1157+30del
ENST00000368300.8:c.1157+28_1157+30del	ENSP00000357283.4:n.1157+28_1157+30del
ENST00000368301.6:c.1157+28_1157+30del	ENSP00000357284.2:n.1157+28_1157+30del
ENST00000448611.6:c.821+28_821+30del	ENSP00000395597.2:n.821+28_821+30del
ENST00000473598.6:c.860+28_860+30del	ENSP00000421821.1:n.860+28_860+30del
ENST00000496738.5:n.542+28_542+30del
ENST00000498722.2:n.389+28_389+30del
ENST00000508500.1:c.35+28_35+30del	ENSP00000424977.1:n.35+28_35+30del
NM_001257374.2:c.821+28_821+30del	NP_001244303.1:n.821+28_821+30del
NM_001282624.1:c.914+28_914+30del	NP_001269553.1:n.914+28_914+30del
NM_001282625.1:c.1157+28_1157+30del	NP_001269554.1:n.1157+28_1157+30del
NM_001282626.1:c.1157+28_1157+30del	NP_001269555.1:n.1157+28_1157+30del
NM_005572.3:c.1157+28_1157+30del , LRG_254t1:c.1157+28_1157+30del	NP_005563.1:n.1157+28_1157+30del
NM_170707.3:c.1157+28_1157+30del	NP_733821.1:n.1157+28_1157+30del
NM_170708.3:c.1157+28_1157+30del	NP_733822.1:n.1157+28_1157+30del
XM_011509533.1:c.821+28_821+30del	XP_011507835.1:n.821+28_821+30del
XM_011509534.1:c.533+28_533+30del	XP_011507836.1:n.533+28_533+30del
XR_921781.1:n.1446+28_1446+30del
XM_011509534.2:c.533+28_533+30del	XP_011507836.1:n.533+28_533+30del
XR_921781.2:n.1444+28_1444+30del
NM_170707.4:c.1157+28_1157+30del MANE Select	NP_733821.1:n.1157+28_1157+30del
NM_001257374.3:c.821+28_821+30del	NP_001244303.1:n.821+28_821+30del
NM_001282626.2:c.1157+28_1157+30del	NP_001269555.1:n.1157+28_1157+30del
NM_001282624.2:c.914+28_914+30del	NP_001269553.1:n.914+28_914+30del
NM_001282625.2:c.1157+28_1157+30del	NP_001269554.1:n.1157+28_1157+30del
NM_005572.4:c.1157+28_1157+30del MANE Plus Clinical	NP_005563.1:n.1157+28_1157+30del
NM_170708.4:c.1157+28_1157+30del	NP_733822.1:n.1157+28_1157+30del