Canonical Allele Identifier: CA1140661085

Gene: LMNA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156137118G= , CM000663.2:g.156137118G=	GRCh38
NC_000001.10:g.156106909G= , CM000663.1:g.156106909G=	GRCh37
NC_000001.9:g.154373533G=	NCBI36
NG_008692.2:g.59546G= , LRG_254:g.59546G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000504687.7:c.936G=	ENSP00000426535.3:p.Trp312=
ENST00000459904.2:n.742G=
ENST00000498722.3:n.726G=
ENST00000682650.1:c.1494G=	ENSP00000506904.1:p.Trp498=
ENST00000683032.1:c.1494G=	ENSP00000506771.1:p.Trp498=
ENST00000684195.1:c.1494G=	ENSP00000508220.1:p.Trp498=
ENST00000361308.9:c.1494G=	ENSP00000355292.6:p.Trp498=
ENST00000368300.9:c.1494G= MANE Select	ENSP00000357283.4:p.Trp498=
ENST00000496738.6:n.1953G=
ENST00000674518.1:c.*844G=	ENSP00000502261.1:n.*844G=
ENST00000674600.1:c.*1293G=	ENSP00000501666.1:n.*1293G=
ENST00000674720.1:c.*56G=	ENSP00000502798.1:n.*56G=
ENST00000675431.1:n.1187G=
ENST00000675455.1:c.*1294G=	ENSP00000501795.1:n.*1294G=
ENST00000675667.1:c.1494G=	ENSP00000501803.1:p.Trp498=
ENST00000675874.1:c.*965G=	ENSP00000501851.1:n.*965G=
ENST00000675881.1:c.*505G=	ENSP00000501670.1:n.*505G=
ENST00000675939.1:c.1494G=	ENSP00000502256.1:p.Trp498=
ENST00000675989.1:n.2353G=
ENST00000676208.1:c.*597G=	ENSP00000502468.1:n.*597G=
ENST00000676283.1:n.1869G=
ENST00000676385.2:c.1494G=	ENSP00000502091.1:p.Trp498=
ENST00000676434.1:c.*505G=	ENSP00000501648.1:n.*505G=
ENST00000677389.1:c.1494G= MANE Plus Clinical	ENSP00000503633.1:p.Trp498=
ENST00000347559.6:c.1494G=	ENSP00000292304.3:p.Trp498=
ENST00000361308.8:c.1312-73G=	ENSP00000355292.5:n.1312-73G=
ENST00000368297.5:c.1251G=	ENSP00000357280.1:p.Trp417=
ENST00000368298.2:n.1326G=
ENST00000368299.7:c.1494G=	ENSP00000357282.3:p.Trp498=
ENST00000368300.8:c.1494G=	ENSP00000357283.4:p.Trp498=
ENST00000368301.6:c.1494G=	ENSP00000357284.2:p.Trp498=
ENST00000448611.6:c.1158G=	ENSP00000395597.2:p.Trp386=
ENST00000459904.1:n.742G=
ENST00000473598.6:c.1197G=	ENSP00000421821.1:p.Trp399=
ENST00000496738.5:n.963G=
ENST00000498722.2:n.726G=
ENST00000508500.1:c.372G=	ENSP00000424977.1:p.Trp124=
NM_001257374.2:c.1158G=	NP_001244303.1:p.Trp386=
NM_001282624.1:c.1251G=	NP_001269553.1:p.Trp417=
NM_001282625.1:c.1494G=	NP_001269554.1:p.Trp498=
NM_001282626.1:c.1494G=	NP_001269555.1:p.Trp498=
NM_005572.3:c.1494G= , LRG_254t1:c.1494G=	NP_005563.1:p.Trp498=
NM_170707.3:c.1494G=	NP_733821.1:p.Trp498=
NM_170708.3:c.1494G=	NP_733822.1:p.Trp498=
XM_011509533.1:c.1158G=	XP_011507835.1:p.Trp386=
XM_011509534.1:c.870G=	XP_011507836.1:p.Trp290=
XR_921781.1:n.1783G=
XM_011509534.2:c.870G=	XP_011507836.1:p.Trp290=
XR_921781.2:n.1781G=
NM_170707.4:c.1494G= MANE Select	NP_733821.1:p.Trp498=
NM_001257374.3:c.1158G=	NP_001244303.1:p.Trp386=
NM_001282626.2:c.1494G=	NP_001269555.1:p.Trp498=
NM_001282624.2:c.1251G=	NP_001269553.1:p.Trp417=
NM_001282625.2:c.1494G=	NP_001269554.1:p.Trp498=
NM_005572.4:c.1494G= MANE Plus Clinical	NP_005563.1:p.Trp498=
NM_170708.4:c.1494G=	NP_733822.1:p.Trp498=