Canonical Allele Identifier: CA2586964217

Gene: LMNA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156136167del , CM000663.2:g.156136167del	GRCh38
NC_000001.10:g.156105958del , CM000663.1:g.156105958del	GRCh37
NC_000001.9:g.154372582del	NCBI36
NG_008692.2:g.58595del , LRG_254:g.58595del

Transcript Alleles

HGVS	Amino-acid change
ENST00000504687.7:c.600-47del	ENSP00000426535.3:n.600-47del
ENST00000498722.3:n.390-47del
ENST00000682650.1:c.1158-47del	ENSP00000506904.1:n.1158-47del
ENST00000683032.1:c.1158-47del	ENSP00000506771.1:n.1158-47del
ENST00000684195.1:c.1158-47del	ENSP00000508220.1:n.1158-47del
ENST00000361308.9:c.1158-47del	ENSP00000355292.6:n.1158-47del
ENST00000368300.9:c.1158-47del MANE Select	ENSP00000357283.4:n.1158-47del
ENST00000496738.6:n.1533-47del
ENST00000674518.1:c.*508-47del	ENSP00000502261.1:n.*508-47del
ENST00000674600.1:c.*957-47del	ENSP00000501666.1:n.*957-47del
ENST00000674720.1:c.1158-47del	ENSP00000502798.1:n.1158-47del
ENST00000675431.1:n.851-47del
ENST00000675455.1:c.*958-47del	ENSP00000501795.1:n.*958-47del
ENST00000675667.1:c.1158-47del	ENSP00000501803.1:n.1158-47del
ENST00000675874.1:c.*629-47del	ENSP00000501851.1:n.*629-47del
ENST00000675881.1:c.*169-47del	ENSP00000501670.1:n.*169-47del
ENST00000675939.1:c.1158-47del	ENSP00000502256.1:n.1158-47del
ENST00000675989.1:n.1533-47del
ENST00000676208.1:c.*214del	ENSP00000502468.1:n.*214del
ENST00000676283.1:n.1533-47del
ENST00000676385.2:c.1158-47del	ENSP00000502091.1:n.1158-47del
ENST00000676434.1:c.*169-47del	ENSP00000501648.1:n.*169-47del
ENST00000677389.1:c.1158-47del MANE Plus Clinical	ENSP00000503633.1:n.1158-47del
ENST00000347559.6:c.1158-47del	ENSP00000292304.3:n.1158-47del
ENST00000361308.8:c.1158-47del	ENSP00000355292.5:n.1158-47del
ENST00000368297.5:c.915-47del	ENSP00000357280.1:n.915-47del
ENST00000368298.2:n.422-47del
ENST00000368299.7:c.1158-47del	ENSP00000357282.3:n.1158-47del
ENST00000368300.8:c.1158-47del	ENSP00000357283.4:n.1158-47del
ENST00000368301.6:c.1158-47del	ENSP00000357284.2:n.1158-47del
ENST00000448611.6:c.822-47del	ENSP00000395597.2:n.822-47del
ENST00000473598.6:c.861-47del	ENSP00000421821.1:n.861-47del
ENST00000496738.5:n.543-47del
ENST00000498722.2:n.390-47del
ENST00000508500.1:c.36-47del	ENSP00000424977.1:n.36-47del
NM_001257374.2:c.822-47del	NP_001244303.1:n.822-47del
NM_001282624.1:c.915-47del	NP_001269553.1:n.915-47del
NM_001282625.1:c.1158-47del	NP_001269554.1:n.1158-47del
NM_001282626.1:c.1158-47del	NP_001269555.1:n.1158-47del
NM_005572.3:c.1158-47del , LRG_254t1:c.1158-47del	NP_005563.1:n.1158-47del
NM_170707.3:c.1158-47del	NP_733821.1:n.1158-47del
NM_170708.3:c.1158-47del	NP_733822.1:n.1158-47del
XM_011509533.1:c.822-47del	XP_011507835.1:n.822-47del
XM_011509534.1:c.534-47del	XP_011507836.1:n.534-47del
XR_921781.1:n.1447-47del
XM_011509534.2:c.534-47del	XP_011507836.1:n.534-47del
XR_921781.2:n.1445-47del
NM_170707.4:c.1158-47del MANE Select	NP_733821.1:n.1158-47del
NM_001257374.3:c.822-47del	NP_001244303.1:n.822-47del
NM_001282626.2:c.1158-47del	NP_001269555.1:n.1158-47del
NM_001282624.2:c.915-47del	NP_001269553.1:n.915-47del
NM_001282625.2:c.1158-47del	NP_001269554.1:n.1158-47del
NM_005572.4:c.1158-47del MANE Plus Clinical	NP_005563.1:n.1158-47del
NM_170708.4:c.1158-47del	NP_733822.1:n.1158-47del