Canonical Allele Identifier: CA1140680165
Gene: LMNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156136413C= , CM000663.2:g.156136413C= GRCh38
NC_000001.10:g.156106204C= , CM000663.1:g.156106204C= GRCh37
NC_000001.9:g.154372828C= NCBI36
NG_008692.2:g.58841C= , LRG_254:g.58841C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504687.7:c.799C= ENSP00000426535.3:p.Arg267=
ENST00000459904.2:n.121C=
ENST00000498722.3:n.589C=
ENST00000682650.1:c.1357C= ENSP00000506904.1:p.Arg453=
ENST00000683032.1:c.1357C= ENSP00000506771.1:p.Arg453=
ENST00000684195.1:c.1357C= ENSP00000508220.1:p.Arg453=
ENST00000361308.9:c.1357C= ENSP00000355292.6:p.Arg453=
ENST00000368300.9:c.1357C= MANE Select ENSP00000357283.4:p.Arg453=
ENST00000496738.6:n.1732C=
ENST00000674518.1:c.*707C= ENSP00000502261.1:n.*707C=
ENST00000674600.1:c.*1156C= ENSP00000501666.1:n.*1156C=
ENST00000674720.1:c.1357C= ENSP00000502798.1:p.Arg453=
ENST00000675431.1:n.1050C=
ENST00000675455.1:c.*1157C= ENSP00000501795.1:n.*1157C=
ENST00000675667.1:c.1357C= ENSP00000501803.1:p.Arg453=
ENST00000675874.1:c.*828C= ENSP00000501851.1:n.*828C=
ENST00000675881.1:c.*368C= ENSP00000501670.1:n.*368C=
ENST00000675939.1:c.1357C= ENSP00000502256.1:p.Arg453=
ENST00000675989.1:n.1732C=
ENST00000676208.1:c.*460C= ENSP00000502468.1:n.*460C=
ENST00000676283.1:n.1732C=
ENST00000676385.2:c.1357C= ENSP00000502091.1:p.Arg453=
ENST00000676434.1:c.*368C= ENSP00000501648.1:n.*368C=
ENST00000677389.1:c.1357C= MANE Plus Clinical ENSP00000503633.1:p.Arg453=
ENST00000347559.6:c.1357C= ENSP00000292304.3:p.Arg453=
ENST00000361308.8:c.1311+46C= ENSP00000355292.5:n.1311+46C=
ENST00000368297.5:c.1114C= ENSP00000357280.1:p.Arg372=
ENST00000368298.2:n.621C=
ENST00000368299.7:c.1357C= ENSP00000357282.3:p.Arg453=
ENST00000368300.8:c.1357C= ENSP00000357283.4:p.Arg453=
ENST00000368301.6:c.1357C= ENSP00000357284.2:p.Arg453=
ENST00000448611.6:c.1021C= ENSP00000395597.2:p.Arg341=
ENST00000459904.1:n.121C=
ENST00000473598.6:c.1060C= ENSP00000421821.1:p.Arg354=
ENST00000496738.5:n.742C=
ENST00000498722.2:n.589C=
ENST00000508500.1:c.235C= ENSP00000424977.1:p.Arg79=
NM_001257374.2:c.1021C= NP_001244303.1:p.Arg341=
NM_001282624.1:c.1114C= NP_001269553.1:p.Arg372=
NM_001282625.1:c.1357C= NP_001269554.1:p.Arg453=
NM_001282626.1:c.1357C= NP_001269555.1:p.Arg453=
NM_005572.3:c.1357C= , LRG_254t1:c.1357C= NP_005563.1:p.Arg453=
NM_170707.3:c.1357C= NP_733821.1:p.Arg453=
NM_170708.3:c.1357C= NP_733822.1:p.Arg453=
XM_011509533.1:c.1021C= XP_011507835.1:p.Arg341=
XM_011509534.1:c.733C= XP_011507836.1:p.Arg245=
XR_921781.1:n.1646C=
XM_011509534.2:c.733C= XP_011507836.1:p.Arg245=
XR_921781.2:n.1644C=
NM_170707.4:c.1357C= MANE Select NP_733821.1:p.Arg453=
NM_001257374.3:c.1021C= NP_001244303.1:p.Arg341=
NM_001282626.2:c.1357C= NP_001269555.1:p.Arg453=
NM_001282624.2:c.1114C= NP_001269553.1:p.Arg372=
NM_001282625.2:c.1357C= NP_001269554.1:p.Arg453=
NM_005572.4:c.1357C= MANE Plus Clinical NP_005563.1:p.Arg453=
NM_170708.4:c.1357C= NP_733822.1:p.Arg453=