Canonical Allele Identifier: CA2740098418
Gene: LMNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156137209dup , CM000663.2:g.156137209dup GRCh38
NC_000001.10:g.156107000dup , CM000663.1:g.156107000dup GRCh37
NC_000001.9:g.154373624dup NCBI36
NG_008692.2:g.59637dup , LRG_254:g.59637dup

Transcript Alleles

HGVS Amino-acid change
ENST00000504687.7:c.1027dup ENSP00000426535.3:p.Ala343GlyfsTer23
ENST00000459904.2:n.833dup
ENST00000498722.3:n.817dup
ENST00000682650.1:c.1585dup ENSP00000506904.1:p.Ala529GlyfsTer20
ENST00000683032.1:c.1585dup ENSP00000506771.1:p.Ala529GlyfsTer23
ENST00000684195.1:c.1579+6dup ENSP00000508220.1:n.1579+6dup
ENST00000361308.9:c.1585dup ENSP00000355292.6:p.Ala529GlyfsTer23
ENST00000368300.9:c.1585dup MANE Select ENSP00000357283.4:p.Ala529GlyfsTer23
ENST00000496738.6:n.2044dup
ENST00000674518.1:c.*935dup ENSP00000502261.1:n.*935dup
ENST00000674600.1:c.*1384dup ENSP00000501666.1:n.*1384dup
ENST00000674720.1:c.*147dup ENSP00000502798.1:n.*147dup
ENST00000675431.1:n.1278dup
ENST00000675455.1:c.*1385dup ENSP00000501795.1:n.*1385dup
ENST00000675667.1:c.1585dup ENSP00000501803.1:p.Ala529GlyfsTer23
ENST00000675874.1:c.*1056dup ENSP00000501851.1:n.*1056dup
ENST00000675881.1:c.*596dup ENSP00000501670.1:n.*596dup
ENST00000675939.1:c.1585dup ENSP00000502256.1:p.Ala529GlyfsTer23
ENST00000675989.1:n.2444dup
ENST00000676208.1:c.*688dup ENSP00000502468.1:n.*688dup
ENST00000676283.1:n.1960dup
ENST00000676385.2:c.1585dup ENSP00000502091.1:p.Ala529GlyfsTer20
ENST00000676434.1:c.*596dup ENSP00000501648.1:n.*596dup
ENST00000677389.1:c.1585dup MANE Plus Clinical ENSP00000503633.1:p.Ala529GlyfsTer23
ENST00000347559.6:c.1585dup ENSP00000292304.3:p.Ala529GlyfsTer20
ENST00000361308.8:c.1330dup ENSP00000355292.5:p.Ala444GlyfsTer23
ENST00000368297.5:c.1342dup ENSP00000357280.1:p.Ala448GlyfsTer23
ENST00000368298.2:n.1417dup
ENST00000368299.7:c.1585dup ENSP00000357282.3:p.Ala529GlyfsTer23
ENST00000368300.8:c.1585dup ENSP00000357283.4:p.Ala529GlyfsTer23
ENST00000368301.6:c.1585dup ENSP00000357284.2:p.Ala529GlyfsTer23
ENST00000448611.6:c.1249dup ENSP00000395597.2:p.Ala417GlyfsTer23
ENST00000459904.1:n.833dup
ENST00000473598.6:c.1288dup ENSP00000421821.1:p.Ala430GlyfsTer23
ENST00000496738.5:n.1054dup
ENST00000498722.2:n.817dup
ENST00000508500.1:c.463dup ENSP00000424977.1:p.Ala155GlyfsTer20
NM_001257374.2:c.1249dup NP_001244303.1:p.Ala417GlyfsTer23
NM_001282624.1:c.1342dup NP_001269553.1:p.Ala448GlyfsTer23
NM_001282625.1:c.1585dup NP_001269554.1:p.Ala529GlyfsTer23
NM_001282626.1:c.1585dup NP_001269555.1:p.Ala529GlyfsTer23
NM_005572.3:c.1585dup , LRG_254t1:c.1585dup NP_005563.1:p.Ala529GlyfsTer23
NM_170707.3:c.1585dup NP_733821.1:p.Ala529GlyfsTer23
NM_170708.3:c.1585dup NP_733822.1:p.Ala529GlyfsTer20
XM_011509533.1:c.1249dup XP_011507835.1:p.Ala417GlyfsTer23
XM_011509534.1:c.961dup XP_011507836.1:p.Ala321GlyfsTer23
XR_921781.1:n.1874dup
XM_011509534.2:c.961dup XP_011507836.1:p.Ala321GlyfsTer23
XR_921781.2:n.1872dup
NM_170707.4:c.1585dup MANE Select NP_733821.1:p.Ala529GlyfsTer23
NM_001257374.3:c.1249dup NP_001244303.1:p.Ala417GlyfsTer23
NM_001282626.2:c.1585dup NP_001269555.1:p.Ala529GlyfsTer23
NM_001282624.2:c.1342dup NP_001269553.1:p.Ala448GlyfsTer23
NM_001282625.2:c.1585dup NP_001269554.1:p.Ala529GlyfsTer23
NM_005572.4:c.1585dup MANE Plus Clinical NP_005563.1:p.Ala529GlyfsTer23
NM_170708.4:c.1585dup NP_733822.1:p.Ala529GlyfsTer20