Canonical Allele Identifier: CA1200471300
Gene: LMNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156134479T= , CM000663.2:g.156134479T= GRCh38
NC_000001.10:g.156104270T= , CM000663.1:g.156104270T= GRCh37
NC_000001.9:g.154370894T= NCBI36
NG_008692.2:g.56907T= , LRG_254:g.56907T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504687.7:c.32T= ENSP00000426535.3:p.Leu11=
ENST00000682650.1:c.590T= ENSP00000506904.1:p.Leu197=
ENST00000683032.1:c.590T= ENSP00000506771.1:p.Leu197=
ENST00000684195.1:c.590T= ENSP00000508220.1:p.Leu197=
ENST00000361308.9:c.590T= ENSP00000355292.6:p.Leu197=
ENST00000368300.9:c.590T= MANE Select ENSP00000357283.4:p.Leu197=
ENST00000496738.6:n.965T=
ENST00000504687.6:c.-75T= ENSP00000426535.2:n.-75T=
ENST00000674518.1:c.590T= ENSP00000502261.1:p.Leu197=
ENST00000674600.1:c.*389T= ENSP00000501666.1:n.*389T=
ENST00000674720.1:c.590T= ENSP00000502798.1:p.Leu197=
ENST00000675431.1:n.283T=
ENST00000675455.1:c.*390T= ENSP00000501795.1:n.*390T=
ENST00000675667.1:c.590T= ENSP00000501803.1:p.Leu197=
ENST00000675874.1:c.*61T= ENSP00000501851.1:n.*61T=
ENST00000675881.1:c.590T= ENSP00000501670.1:p.Leu197=
ENST00000675939.1:c.590T= ENSP00000502256.1:p.Leu197=
ENST00000675989.1:n.965T=
ENST00000676208.1:c.590T= ENSP00000502468.1:p.Leu197=
ENST00000676283.1:n.965T=
ENST00000676385.2:c.590T= ENSP00000502091.1:p.Leu197=
ENST00000676434.1:c.590T= ENSP00000501648.1:p.Leu197=
ENST00000677389.1:c.590T= MANE Plus Clinical ENSP00000503633.1:p.Leu197=
ENST00000347559.6:c.590T= ENSP00000292304.3:p.Leu197=
ENST00000361308.8:c.590T= ENSP00000355292.5:p.Leu197=
ENST00000368297.5:c.347T= ENSP00000357280.1:p.Leu116=
ENST00000368299.7:c.590T= ENSP00000357282.3:p.Leu197=
ENST00000368300.8:c.590T= ENSP00000357283.4:p.Leu197=
ENST00000368301.6:c.590T= ENSP00000357284.2:p.Leu197=
ENST00000448611.6:c.254T= ENSP00000395597.2:p.Leu85=
ENST00000470199.2:n.532T=
ENST00000473598.6:c.293T= ENSP00000421821.1:p.Leu98=
ENST00000502357.5:n.488T=
ENST00000502751.5:n.562T=
ENST00000504687.5:c.341T= ENSP00000426535.1:p.Leu114=
ENST00000515459.5:c.*264T= ENSP00000424518.1:n.*264T=
NM_001257374.2:c.254T= NP_001244303.1:p.Leu85=
NM_001282624.1:c.347T= NP_001269553.1:p.Leu116=
NM_001282625.1:c.590T= NP_001269554.1:p.Leu197=
NM_001282626.1:c.590T= NP_001269555.1:p.Leu197=
NM_005572.3:c.590T= , LRG_254t1:c.590T= NP_005563.1:p.Leu197=
NM_170707.3:c.590T= NP_733821.1:p.Leu197=
NM_170708.3:c.590T= NP_733822.1:p.Leu197=
XM_011509533.1:c.254T= XP_011507835.1:p.Leu85=
XM_011509534.1:c.-75T= XP_011507836.1:n.-75T=
XR_921781.1:n.839T=
XM_011509534.2:c.-75T= XP_011507836.1:n.-75T=
XR_921781.2:n.837T=
NM_170707.4:c.590T= MANE Select NP_733821.1:p.Leu197=
NM_001257374.3:c.254T= NP_001244303.1:p.Leu85=
NM_001282626.2:c.590T= NP_001269555.1:p.Leu197=
NM_001282624.2:c.347T= NP_001269553.1:p.Leu116=
NM_001282625.2:c.590T= NP_001269554.1:p.Leu197=
NM_005572.4:c.590T= MANE Plus Clinical NP_005563.1:p.Leu197=
NM_170708.4:c.590T= NP_733822.1:p.Leu197=