Canonical Allele Identifier: CA2648351844
Gene: LMNA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156137783del , CM000663.2:g.156137783del GRCh38
NC_000001.10:g.156107574del , CM000663.1:g.156107574del GRCh37
NC_000001.9:g.154374198del NCBI36
NG_008692.2:g.60211del , LRG_254:g.60211del

Transcript Alleles

HGVS Amino-acid Change
ENST00000504687.7:c.1140+40del ENSP00000426535.3:n.1140+40del
ENST00000498722.3:n.970del
ENST00000682650.1:c.1608+551del ENSP00000506904.1:n.1608+551del
ENST00000683032.1:c.1698+40del ENSP00000506771.1:n.1698+40del
ENST00000683773.1:n.43+40del
ENST00000684195.1:c.*86del ENSP00000508220.1:n.*86del
ENST00000361308.9:c.1698+40del ENSP00000355292.6:n.1698+40del
ENST00000368300.9:c.1698+40del MANE Select ENSP00000357283.4:n.1698+40del
ENST00000496738.6:n.2197del
ENST00000674518.1:c.*1048+40del ENSP00000502261.1:n.*1048+40del
ENST00000674600.1:c.*1497+40del ENSP00000501666.1:n.*1497+40del
ENST00000674720.1:c.*300del ENSP00000502798.1:n.*300del
ENST00000675431.1:n.1431del
ENST00000675455.1:c.*1498+40del ENSP00000501795.1:n.*1498+40del
ENST00000675667.1:c.1698+40del ENSP00000501803.1:n.1698+40del
ENST00000675874.1:c.*1169+40del ENSP00000501851.1:n.*1169+40del
ENST00000675881.1:c.*709+40del ENSP00000501670.1:n.*709+40del
ENST00000675939.1:c.1698+40del ENSP00000502256.1:n.1698+40del
ENST00000675989.1:n.2597del
ENST00000676208.1:c.*801+40del ENSP00000502468.1:n.*801+40del
ENST00000676283.1:n.2534del
ENST00000676385.2:c.1608+551del ENSP00000502091.1:n.1608+551del
ENST00000676434.1:c.*749del ENSP00000501648.1:n.*749del
ENST00000677389.1:c.*19del MANE Plus Clinical ENSP00000503633.1:n.*19del
ENST00000347559.6:c.1608+551del ENSP00000292304.3:n.1608+551del
ENST00000368297.5:c.*19del ENSP00000357280.1:n.*19del
ENST00000368299.7:c.1698+40del ENSP00000357282.3:n.1698+40del
ENST00000368300.8:c.1698+40del ENSP00000357283.4:n.1698+40del
ENST00000368301.6:c.*19del ENSP00000357284.2:n.*19del
ENST00000448611.6:c.1362+40del ENSP00000395597.2:n.1362+40del
ENST00000473598.6:c.1401+40del ENSP00000421821.1:n.1401+40del
ENST00000496738.5:n.1207del
ENST00000498722.2:n.970del
ENST00000506981.1:n.282+40del
ENST00000508500.1:c.486+551del ENSP00000424977.1:n.486+551del
NM_001257374.2:c.1362+40del NP_001244303.1:n.1362+40del
NM_001282624.1:c.*19del NP_001269553.1:n.*19del
NM_001282625.1:c.*19del NP_001269554.1:n.*19del
NM_001282626.1:c.1698+40del NP_001269555.1:n.1698+40del
NM_005572.3:c.*19del , LRG_254t1:c.*19del NP_005563.1:n.*19del
NM_170707.3:c.1698+40del NP_733821.1:n.1698+40del
NM_170708.3:c.1608+551del NP_733822.1:n.1608+551del
XM_011509533.1:c.1362+40del XP_011507835.1:n.1362+40del
XM_011509534.1:c.1074+40del XP_011507836.1:n.1074+40del
XR_921781.1:n.1987+40del
XM_011509534.2:c.1074+40del XP_011507836.1:n.1074+40del
XR_921781.2:n.1985+40del
NM_170707.4:c.1698+40del MANE Select NP_733821.1:n.1698+40del
NM_001257374.3:c.1362+40del NP_001244303.1:n.1362+40del
NM_001282626.2:c.1698+40del NP_001269555.1:n.1698+40del
NM_001282624.2:c.*19del NP_001269553.1:n.*19del
NM_001282625.2:c.*19del NP_001269554.1:n.*19del
NM_005572.4:c.*19del MANE Plus Clinical NP_005563.1:n.*19del
NM_170708.4:c.1608+551del NP_733822.1:n.1608+551del