Canonical Allele Identifier: CA1140685880
Gene: LMNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156135956G= , CM000663.2:g.156135956G= GRCh38
NC_000001.10:g.156105747G= , CM000663.1:g.156105747G= GRCh37
NC_000001.9:g.154372371G= NCBI36
NG_008692.2:g.58384G= , LRG_254:g.58384G=

Transcript Alleles

HGVS Amino-acid change
ENST00000504687.7:c.434G= ENSP00000426535.3:p.Arg145=
ENST00000498722.3:n.224G=
ENST00000682650.1:c.992G= ENSP00000506904.1:p.Arg331=
ENST00000683032.1:c.992G= ENSP00000506771.1:p.Arg331=
ENST00000684195.1:c.992G= ENSP00000508220.1:p.Arg331=
ENST00000361308.9:c.992G= ENSP00000355292.6:p.Arg331=
ENST00000368300.9:c.992G= MANE Select ENSP00000357283.4:p.Arg331=
ENST00000496738.6:n.1367G=
ENST00000674518.1:c.*342G= ENSP00000502261.1:n.*342G=
ENST00000674600.1:c.*791G= ENSP00000501666.1:n.*791G=
ENST00000674720.1:c.992G= ENSP00000502798.1:p.Arg331=
ENST00000675431.1:n.685G=
ENST00000675455.1:c.*792G= ENSP00000501795.1:n.*792G=
ENST00000675667.1:c.992G= ENSP00000501803.1:p.Arg331=
ENST00000675874.1:c.*463G= ENSP00000501851.1:n.*463G=
ENST00000675881.1:c.*3G= ENSP00000501670.1:n.*3G=
ENST00000675939.1:c.992G= ENSP00000502256.1:p.Arg331=
ENST00000675989.1:n.1367G=
ENST00000676208.1:c.*3G= ENSP00000502468.1:n.*3G=
ENST00000676283.1:n.1367G=
ENST00000676385.2:c.992G= ENSP00000502091.1:p.Arg331=
ENST00000676434.1:c.*3G= ENSP00000501648.1:n.*3G=
ENST00000677389.1:c.992G= MANE Plus Clinical ENSP00000503633.1:p.Arg331=
ENST00000347559.6:c.992G= ENSP00000292304.3:p.Arg331=
ENST00000361308.8:c.992G= ENSP00000355292.5:p.Arg331=
ENST00000368297.5:c.749G= ENSP00000357280.1:p.Arg250=
ENST00000368298.2:n.256G=
ENST00000368299.7:c.992G= ENSP00000357282.3:p.Arg331=
ENST00000368300.8:c.992G= ENSP00000357283.4:p.Arg331=
ENST00000368301.6:c.992G= ENSP00000357284.2:p.Arg331=
ENST00000448611.6:c.656G= ENSP00000395597.2:p.Arg219=
ENST00000473598.6:c.695G= ENSP00000421821.1:p.Arg232=
ENST00000496738.5:n.377G=
ENST00000498722.2:n.224G=
NM_001257374.2:c.656G= NP_001244303.1:p.Arg219=
NM_001282624.1:c.749G= NP_001269553.1:p.Arg250=
NM_001282625.1:c.992G= NP_001269554.1:p.Arg331=
NM_001282626.1:c.992G= NP_001269555.1:p.Arg331=
NM_005572.3:c.992G= , LRG_254t1:c.992G= NP_005563.1:p.Arg331=
NM_170707.3:c.992G= NP_733821.1:p.Arg331=
NM_170708.3:c.992G= NP_733822.1:p.Arg331=
XM_011509533.1:c.656G= XP_011507835.1:p.Arg219=
XM_011509534.1:c.368G= XP_011507836.1:p.Arg123=
XR_921781.1:n.1281G=
XM_011509534.2:c.368G= XP_011507836.1:p.Arg123=
XR_921781.2:n.1279G=
NM_170707.4:c.992G= MANE Select NP_733821.1:p.Arg331=
NM_001257374.3:c.656G= NP_001244303.1:p.Arg219=
NM_001282626.2:c.992G= NP_001269555.1:p.Arg331=
NM_001282624.2:c.749G= NP_001269553.1:p.Arg250=
NM_001282625.2:c.992G= NP_001269554.1:p.Arg331=
NM_005572.4:c.992G= MANE Plus Clinical NP_005563.1:p.Arg331=
NM_170708.4:c.992G= NP_733822.1:p.Arg331=