Canonical Allele Identifier: CA1200473123
Gene: LMNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156137663A= , CM000663.2:g.156137663A= GRCh38
NC_000001.10:g.156107454A= , CM000663.1:g.156107454A= GRCh37
NC_000001.9:g.154374078A= NCBI36
NG_008692.2:g.60091A= , LRG_254:g.60091A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504687.7:c.1060A= ENSP00000426535.3:p.Met354=
ENST00000498722.3:n.850A=
ENST00000682650.1:c.1608+431A= ENSP00000506904.1:n.1608+431A=
ENST00000683032.1:c.1618A= ENSP00000506771.1:p.Met540=
ENST00000684195.1:c.1589A= ENSP00000508220.1:p.His530=
ENST00000361308.9:c.1618A= ENSP00000355292.6:p.Met540=
ENST00000368300.9:c.1618A= MANE Select ENSP00000357283.4:p.Met540=
ENST00000496738.6:n.2077A=
ENST00000674518.1:c.*968A= ENSP00000502261.1:n.*968A=
ENST00000674600.1:c.*1417A= ENSP00000501666.1:n.*1417A=
ENST00000674720.1:c.*180A= ENSP00000502798.1:n.*180A=
ENST00000675431.1:n.1311A=
ENST00000675455.1:c.*1418A= ENSP00000501795.1:n.*1418A=
ENST00000675667.1:c.1618A= ENSP00000501803.1:p.Met540=
ENST00000675874.1:c.*1089A= ENSP00000501851.1:n.*1089A=
ENST00000675881.1:c.*629A= ENSP00000501670.1:n.*629A=
ENST00000675939.1:c.1618A= ENSP00000502256.1:p.Met540=
ENST00000675989.1:n.2477A=
ENST00000676208.1:c.*721A= ENSP00000502468.1:n.*721A=
ENST00000676283.1:n.2414A=
ENST00000676385.2:c.1608+431A= ENSP00000502091.1:n.1608+431A=
ENST00000676434.1:c.*629A= ENSP00000501648.1:n.*629A=
ENST00000677389.1:c.1618A= MANE Plus Clinical ENSP00000503633.1:p.Met540=
ENST00000347559.6:c.1608+431A= ENSP00000292304.3:n.1608+431A=
ENST00000361308.8:c.1363A= ENSP00000355292.5:p.Met455=
ENST00000368297.5:c.1375A= ENSP00000357280.1:p.Met459=
ENST00000368299.7:c.1618A= ENSP00000357282.3:p.Met540=
ENST00000368300.8:c.1618A= ENSP00000357283.4:p.Met540=
ENST00000368301.6:c.1618A= ENSP00000357284.2:p.Met540=
ENST00000448611.6:c.1282A= ENSP00000395597.2:p.Met428=
ENST00000473598.6:c.1321A= ENSP00000421821.1:p.Met441=
ENST00000496738.5:n.1087A=
ENST00000498722.2:n.850A=
ENST00000506981.1:n.202A=
ENST00000508500.1:c.486+431A= ENSP00000424977.1:n.486+431A=
NM_001257374.2:c.1282A= NP_001244303.1:p.Met428=
NM_001282624.1:c.1375A= NP_001269553.1:p.Met459=
NM_001282625.1:c.1618A= NP_001269554.1:p.Met540=
NM_001282626.1:c.1618A= NP_001269555.1:p.Met540=
NM_005572.3:c.1618A= , LRG_254t1:c.1618A= NP_005563.1:p.Met540=
NM_170707.3:c.1618A= NP_733821.1:p.Met540=
NM_170708.3:c.1608+431A= NP_733822.1:n.1608+431A=
XM_011509533.1:c.1282A= XP_011507835.1:p.Met428=
XM_011509534.1:c.994A= XP_011507836.1:p.Met332=
XR_921781.1:n.1907A=
XM_011509534.2:c.994A= XP_011507836.1:p.Met332=
XR_921781.2:n.1905A=
NM_170707.4:c.1618A= MANE Select NP_733821.1:p.Met540=
NM_001257374.3:c.1282A= NP_001244303.1:p.Met428=
NM_001282626.2:c.1618A= NP_001269555.1:p.Met540=
NM_001282624.2:c.1375A= NP_001269553.1:p.Met459=
NM_001282625.2:c.1618A= NP_001269554.1:p.Met540=
NM_005572.4:c.1618A= MANE Plus Clinical NP_005563.1:p.Met540=
NM_170708.4:c.1608+431A= NP_733822.1:n.1608+431A=