Canonical Allele Identifier: CA1143405742
Gene: LMNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156136930A= , CM000663.2:g.156136930A= GRCh38
NC_000001.10:g.156106721A= , CM000663.1:g.156106721A= GRCh37
NC_000001.9:g.154373345A= NCBI36
NG_008692.2:g.59358A= , LRG_254:g.59358A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504687.7:c.832A= ENSP00000426535.3:p.Met278=
ENST00000459904.2:n.638A=
ENST00000498722.3:n.622A=
ENST00000682650.1:c.1390A= ENSP00000506904.1:p.Met464=
ENST00000683032.1:c.1390A= ENSP00000506771.1:p.Met464=
ENST00000684195.1:c.1390A= ENSP00000508220.1:p.Met464=
ENST00000361308.9:c.1390A= ENSP00000355292.6:p.Met464=
ENST00000368300.9:c.1390A= MANE Select ENSP00000357283.4:p.Met464=
ENST00000496738.6:n.1765A=
ENST00000674518.1:c.*740A= ENSP00000502261.1:n.*740A=
ENST00000674600.1:c.*1189A= ENSP00000501666.1:n.*1189A=
ENST00000674720.1:c.1503A= ENSP00000502798.1:p.Pro501=
ENST00000675431.1:n.1083A=
ENST00000675455.1:c.*1190A= ENSP00000501795.1:n.*1190A=
ENST00000675667.1:c.1390A= ENSP00000501803.1:p.Met464=
ENST00000675874.1:c.*861A= ENSP00000501851.1:n.*861A=
ENST00000675881.1:c.*401A= ENSP00000501670.1:n.*401A=
ENST00000675939.1:c.1390A= ENSP00000502256.1:p.Met464=
ENST00000675989.1:n.2249A=
ENST00000676208.1:c.*493A= ENSP00000502468.1:n.*493A=
ENST00000676283.1:n.1765A=
ENST00000676385.2:c.1390A= ENSP00000502091.1:p.Met464=
ENST00000676434.1:c.*401A= ENSP00000501648.1:n.*401A=
ENST00000677389.1:c.1390A= MANE Plus Clinical ENSP00000503633.1:p.Met464=
ENST00000347559.6:c.1390A= ENSP00000292304.3:p.Met464=
ENST00000361308.8:c.1312-261A= ENSP00000355292.5:n.1312-261A=
ENST00000368297.5:c.1147A= ENSP00000357280.1:p.Met383=
ENST00000368298.2:n.1138A=
ENST00000368299.7:c.1390A= ENSP00000357282.3:p.Met464=
ENST00000368300.8:c.1390A= ENSP00000357283.4:p.Met464=
ENST00000368301.6:c.1390A= ENSP00000357284.2:p.Met464=
ENST00000448611.6:c.1054A= ENSP00000395597.2:p.Met352=
ENST00000459904.1:n.638A=
ENST00000473598.6:c.1093A= ENSP00000421821.1:p.Met365=
ENST00000496738.5:n.775A=
ENST00000498722.2:n.622A=
ENST00000508500.1:c.268A= ENSP00000424977.1:p.Met90=
NM_001257374.2:c.1054A= NP_001244303.1:p.Met352=
NM_001282624.1:c.1147A= NP_001269553.1:p.Met383=
NM_001282625.1:c.1390A= NP_001269554.1:p.Met464=
NM_001282626.1:c.1390A= NP_001269555.1:p.Met464=
NM_005572.3:c.1390A= , LRG_254t1:c.1390A= NP_005563.1:p.Met464=
NM_170707.3:c.1390A= NP_733821.1:p.Met464=
NM_170708.3:c.1390A= NP_733822.1:p.Met464=
XM_011509533.1:c.1054A= XP_011507835.1:p.Met352=
XM_011509534.1:c.766A= XP_011507836.1:p.Met256=
XR_921781.1:n.1679A=
XM_011509534.2:c.766A= XP_011507836.1:p.Met256=
XR_921781.2:n.1677A=
NM_170707.4:c.1390A= MANE Select NP_733821.1:p.Met464=
NM_001257374.3:c.1054A= NP_001244303.1:p.Met352=
NM_001282626.2:c.1390A= NP_001269555.1:p.Met464=
NM_001282624.2:c.1147A= NP_001269553.1:p.Met383=
NM_001282625.2:c.1390A= NP_001269554.1:p.Met464=
NM_005572.4:c.1390A= MANE Plus Clinical NP_005563.1:p.Met464=
NM_170708.4:c.1390A= NP_733822.1:p.Met464=