Canonical Allele Identifier: CA1200473127
Gene: LMNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156137673T= , CM000663.2:g.156137673T= GRCh38
NC_000001.10:g.156107464T= , CM000663.1:g.156107464T= GRCh37
NC_000001.9:g.154374088T= NCBI36
NG_008692.2:g.60101T= , LRG_254:g.60101T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504687.7:c.1070T= ENSP00000426535.3:p.Leu357=
ENST00000498722.3:n.860T=
ENST00000682650.1:c.1608+441T= ENSP00000506904.1:n.1608+441T=
ENST00000683032.1:c.1628T= ENSP00000506771.1:p.Leu543=
ENST00000684195.1:c.1599T= ENSP00000508220.1:p.Ala533=
ENST00000361308.9:c.1628T= ENSP00000355292.6:p.Leu543=
ENST00000368300.9:c.1628T= MANE Select ENSP00000357283.4:p.Leu543=
ENST00000496738.6:n.2087T=
ENST00000674518.1:c.*978T= ENSP00000502261.1:n.*978T=
ENST00000674600.1:c.*1427T= ENSP00000501666.1:n.*1427T=
ENST00000674720.1:c.*190T= ENSP00000502798.1:n.*190T=
ENST00000675431.1:n.1321T=
ENST00000675455.1:c.*1428T= ENSP00000501795.1:n.*1428T=
ENST00000675667.1:c.1628T= ENSP00000501803.1:p.Leu543=
ENST00000675874.1:c.*1099T= ENSP00000501851.1:n.*1099T=
ENST00000675881.1:c.*639T= ENSP00000501670.1:n.*639T=
ENST00000675939.1:c.1628T= ENSP00000502256.1:p.Leu543=
ENST00000675989.1:n.2487T=
ENST00000676208.1:c.*731T= ENSP00000502468.1:n.*731T=
ENST00000676283.1:n.2424T=
ENST00000676385.2:c.1608+441T= ENSP00000502091.1:n.1608+441T=
ENST00000676434.1:c.*639T= ENSP00000501648.1:n.*639T=
ENST00000677389.1:c.1628T= MANE Plus Clinical ENSP00000503633.1:p.Leu543=
ENST00000347559.6:c.1608+441T= ENSP00000292304.3:n.1608+441T=
ENST00000361308.8:c.1373T= ENSP00000355292.5:p.Leu458=
ENST00000368297.5:c.1385T= ENSP00000357280.1:p.Leu462=
ENST00000368299.7:c.1628T= ENSP00000357282.3:p.Leu543=
ENST00000368300.8:c.1628T= ENSP00000357283.4:p.Leu543=
ENST00000368301.6:c.1628T= ENSP00000357284.2:p.Leu543=
ENST00000448611.6:c.1292T= ENSP00000395597.2:p.Leu431=
ENST00000473598.6:c.1331T= ENSP00000421821.1:p.Leu444=
ENST00000496738.5:n.1097T=
ENST00000498722.2:n.860T=
ENST00000506981.1:n.212T=
ENST00000508500.1:c.486+441T= ENSP00000424977.1:n.486+441T=
NM_001257374.2:c.1292T= NP_001244303.1:p.Leu431=
NM_001282624.1:c.1385T= NP_001269553.1:p.Leu462=
NM_001282625.1:c.1628T= NP_001269554.1:p.Leu543=
NM_001282626.1:c.1628T= NP_001269555.1:p.Leu543=
NM_005572.3:c.1628T= , LRG_254t1:c.1628T= NP_005563.1:p.Leu543=
NM_170707.3:c.1628T= NP_733821.1:p.Leu543=
NM_170708.3:c.1608+441T= NP_733822.1:n.1608+441T=
XM_011509533.1:c.1292T= XP_011507835.1:p.Leu431=
XM_011509534.1:c.1004T= XP_011507836.1:p.Leu335=
XR_921781.1:n.1917T=
XM_011509534.2:c.1004T= XP_011507836.1:p.Leu335=
XR_921781.2:n.1915T=
NM_170707.4:c.1628T= MANE Select NP_733821.1:p.Leu543=
NM_001257374.3:c.1292T= NP_001244303.1:p.Leu431=
NM_001282626.2:c.1628T= NP_001269555.1:p.Leu543=
NM_001282624.2:c.1385T= NP_001269553.1:p.Leu462=
NM_001282625.2:c.1628T= NP_001269554.1:p.Leu543=
NM_005572.4:c.1628T= MANE Plus Clinical NP_005563.1:p.Leu543=
NM_170708.4:c.1608+441T= NP_733822.1:n.1608+441T=