Canonical Allele Identifier: CA1200472811
Gene: LMNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156136932G= , CM000663.2:g.156136932G= GRCh38
NC_000001.10:g.156106723G= , CM000663.1:g.156106723G= GRCh37
NC_000001.9:g.154373347G= NCBI36
NG_008692.2:g.59360G= , LRG_254:g.59360G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504687.7:c.834G= ENSP00000426535.3:p.Met278=
ENST00000459904.2:n.640G=
ENST00000498722.3:n.624G=
ENST00000682650.1:c.1392G= ENSP00000506904.1:p.Met464=
ENST00000683032.1:c.1392G= ENSP00000506771.1:p.Met464=
ENST00000684195.1:c.1392G= ENSP00000508220.1:p.Met464=
ENST00000361308.9:c.1392G= ENSP00000355292.6:p.Met464=
ENST00000368300.9:c.1392G= MANE Select ENSP00000357283.4:p.Met464=
ENST00000496738.6:n.1767G=
ENST00000674518.1:c.*742G= ENSP00000502261.1:n.*742G=
ENST00000674600.1:c.*1191G= ENSP00000501666.1:n.*1191G=
ENST00000674720.1:c.1505G= ENSP00000502798.1:p.Trp502=
ENST00000675431.1:n.1085G=
ENST00000675455.1:c.*1192G= ENSP00000501795.1:n.*1192G=
ENST00000675667.1:c.1392G= ENSP00000501803.1:p.Met464=
ENST00000675874.1:c.*863G= ENSP00000501851.1:n.*863G=
ENST00000675881.1:c.*403G= ENSP00000501670.1:n.*403G=
ENST00000675939.1:c.1392G= ENSP00000502256.1:p.Met464=
ENST00000675989.1:n.2251G=
ENST00000676208.1:c.*495G= ENSP00000502468.1:n.*495G=
ENST00000676283.1:n.1767G=
ENST00000676385.2:c.1392G= ENSP00000502091.1:p.Met464=
ENST00000676434.1:c.*403G= ENSP00000501648.1:n.*403G=
ENST00000677389.1:c.1392G= MANE Plus Clinical ENSP00000503633.1:p.Met464=
ENST00000347559.6:c.1392G= ENSP00000292304.3:p.Met464=
ENST00000361308.8:c.1312-259G= ENSP00000355292.5:n.1312-259G=
ENST00000368297.5:c.1149G= ENSP00000357280.1:p.Met383=
ENST00000368298.2:n.1140G=
ENST00000368299.7:c.1392G= ENSP00000357282.3:p.Met464=
ENST00000368300.8:c.1392G= ENSP00000357283.4:p.Met464=
ENST00000368301.6:c.1392G= ENSP00000357284.2:p.Met464=
ENST00000448611.6:c.1056G= ENSP00000395597.2:p.Met352=
ENST00000459904.1:n.640G=
ENST00000473598.6:c.1095G= ENSP00000421821.1:p.Met365=
ENST00000496738.5:n.777G=
ENST00000498722.2:n.624G=
ENST00000508500.1:c.270G= ENSP00000424977.1:p.Met90=
NM_001257374.2:c.1056G= NP_001244303.1:p.Met352=
NM_001282624.1:c.1149G= NP_001269553.1:p.Met383=
NM_001282625.1:c.1392G= NP_001269554.1:p.Met464=
NM_001282626.1:c.1392G= NP_001269555.1:p.Met464=
NM_005572.3:c.1392G= , LRG_254t1:c.1392G= NP_005563.1:p.Met464=
NM_170707.3:c.1392G= NP_733821.1:p.Met464=
NM_170708.3:c.1392G= NP_733822.1:p.Met464=
XM_011509533.1:c.1056G= XP_011507835.1:p.Met352=
XM_011509534.1:c.768G= XP_011507836.1:p.Met256=
XR_921781.1:n.1681G=
XM_011509534.2:c.768G= XP_011507836.1:p.Met256=
XR_921781.2:n.1679G=
NM_170707.4:c.1392G= MANE Select NP_733821.1:p.Met464=
NM_001257374.3:c.1056G= NP_001244303.1:p.Met352=
NM_001282626.2:c.1392G= NP_001269555.1:p.Met464=
NM_001282624.2:c.1149G= NP_001269553.1:p.Met383=
NM_001282625.2:c.1392G= NP_001269554.1:p.Met464=
NM_005572.4:c.1392G= MANE Plus Clinical NP_005563.1:p.Met464=
NM_170708.4:c.1392G= NP_733822.1:p.Met464=