Canonical Allele Identifier: CA1143538384
Gene: LMNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156136921G= , CM000663.2:g.156136921G= GRCh38
NC_000001.10:g.156106712G= , CM000663.1:g.156106712G= GRCh37
NC_000001.9:g.154373336G= NCBI36
NG_008692.2:g.59349G= , LRG_254:g.59349G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504687.7:c.823G= ENSP00000426535.3:p.Asp275=
ENST00000459904.2:n.629G=
ENST00000498722.3:n.613G=
ENST00000682650.1:c.1381G= ENSP00000506904.1:p.Asp461=
ENST00000683032.1:c.1381G= ENSP00000506771.1:p.Asp461=
ENST00000684195.1:c.1381G= ENSP00000508220.1:p.Asp461=
ENST00000361308.9:c.1381G= ENSP00000355292.6:p.Asp461=
ENST00000368300.9:c.1381G= MANE Select ENSP00000357283.4:p.Asp461=
ENST00000496738.6:n.1756G=
ENST00000674518.1:c.*731G= ENSP00000502261.1:n.*731G=
ENST00000674600.1:c.*1180G= ENSP00000501666.1:n.*1180G=
ENST00000674720.1:c.1494G= ENSP00000502798.1:p.Gly498=
ENST00000675431.1:n.1074G=
ENST00000675455.1:c.*1181G= ENSP00000501795.1:n.*1181G=
ENST00000675667.1:c.1381G= ENSP00000501803.1:p.Asp461=
ENST00000675874.1:c.*852G= ENSP00000501851.1:n.*852G=
ENST00000675881.1:c.*392G= ENSP00000501670.1:n.*392G=
ENST00000675939.1:c.1381G= ENSP00000502256.1:p.Asp461=
ENST00000675989.1:n.2240G=
ENST00000676208.1:c.*484G= ENSP00000502468.1:n.*484G=
ENST00000676283.1:n.1756G=
ENST00000676385.2:c.1381G= ENSP00000502091.1:p.Asp461=
ENST00000676434.1:c.*392G= ENSP00000501648.1:n.*392G=
ENST00000677389.1:c.1381G= MANE Plus Clinical ENSP00000503633.1:p.Asp461=
ENST00000347559.6:c.1381G= ENSP00000292304.3:p.Asp461=
ENST00000361308.8:c.1312-270G= ENSP00000355292.5:n.1312-270G=
ENST00000368297.5:c.1138G= ENSP00000357280.1:p.Asp380=
ENST00000368298.2:n.1129G=
ENST00000368299.7:c.1381G= ENSP00000357282.3:p.Asp461=
ENST00000368300.8:c.1381G= ENSP00000357283.4:p.Asp461=
ENST00000368301.6:c.1381G= ENSP00000357284.2:p.Asp461=
ENST00000448611.6:c.1045G= ENSP00000395597.2:p.Asp349=
ENST00000459904.1:n.629G=
ENST00000473598.6:c.1084G= ENSP00000421821.1:p.Asp362=
ENST00000496738.5:n.766G=
ENST00000498722.2:n.613G=
ENST00000508500.1:c.259G= ENSP00000424977.1:p.Asp87=
NM_001257374.2:c.1045G= NP_001244303.1:p.Asp349=
NM_001282624.1:c.1138G= NP_001269553.1:p.Asp380=
NM_001282625.1:c.1381G= NP_001269554.1:p.Asp461=
NM_001282626.1:c.1381G= NP_001269555.1:p.Asp461=
NM_005572.3:c.1381G= , LRG_254t1:c.1381G= NP_005563.1:p.Asp461=
NM_170707.3:c.1381G= NP_733821.1:p.Asp461=
NM_170708.3:c.1381G= NP_733822.1:p.Asp461=
XM_011509533.1:c.1045G= XP_011507835.1:p.Asp349=
XM_011509534.1:c.757G= XP_011507836.1:p.Asp253=
XR_921781.1:n.1670G=
XM_011509534.2:c.757G= XP_011507836.1:p.Asp253=
XR_921781.2:n.1668G=
NM_170707.4:c.1381G= MANE Select NP_733821.1:p.Asp461=
NM_001257374.3:c.1045G= NP_001244303.1:p.Asp349=
NM_001282626.2:c.1381G= NP_001269555.1:p.Asp461=
NM_001282624.2:c.1138G= NP_001269553.1:p.Asp380=
NM_001282625.2:c.1381G= NP_001269554.1:p.Asp461=
NM_005572.4:c.1381G= MANE Plus Clinical NP_005563.1:p.Asp461=
NM_170708.4:c.1381G= NP_733822.1:p.Asp461=