Canonical Allele Identifier: CA1144229008

Gene: LMNA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156136093C= , CM000663.2:g.156136093C=	GRCh38
NC_000001.10:g.156105884C= , CM000663.1:g.156105884C=	GRCh37
NC_000001.9:g.154372508C=	NCBI36
NG_008692.2:g.58521C= , LRG_254:g.58521C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.571C=	ENSP00000426535.3:p.Arg191=
ENST00000498722.3:n.361C=
ENST00000682650.1:c.1129C=	ENSP00000506904.1:p.Arg377=
ENST00000683032.1:c.1129C=	ENSP00000506771.1:p.Arg377=
ENST00000684195.1:c.1129C=	ENSP00000508220.1:p.Arg377=
ENST00000361308.9:c.1129C=	ENSP00000355292.6:p.Arg377=
ENST00000368300.9:c.1129C= MANE Select	ENSP00000357283.4:p.Arg377=
ENST00000496738.6:n.1504C=
ENST00000674518.1:c.*479C=	ENSP00000502261.1:n.*479C=
ENST00000674600.1:c.*928C=	ENSP00000501666.1:n.*928C=
ENST00000674720.1:c.1129C=	ENSP00000502798.1:p.Arg377=
ENST00000675431.1:n.822C=
ENST00000675455.1:c.*929C=	ENSP00000501795.1:n.*929C=
ENST00000675667.1:c.1129C=	ENSP00000501803.1:p.Arg377=
ENST00000675874.1:c.*600C=	ENSP00000501851.1:n.*600C=
ENST00000675881.1:c.*140C=	ENSP00000501670.1:n.*140C=
ENST00000675939.1:c.1129C=	ENSP00000502256.1:p.Arg377=
ENST00000675989.1:n.1504C=
ENST00000676208.1:c.*140C=	ENSP00000502468.1:n.*140C=
ENST00000676283.1:n.1504C=
ENST00000676385.2:c.1129C=	ENSP00000502091.1:p.Arg377=
ENST00000676434.1:c.*140C=	ENSP00000501648.1:n.*140C=
ENST00000677389.1:c.1129C= MANE Plus Clinical	ENSP00000503633.1:p.Arg377=
ENST00000347559.6:c.1129C=	ENSP00000292304.3:p.Arg377=
ENST00000361308.8:c.1129C=	ENSP00000355292.5:p.Arg377=
ENST00000368297.5:c.886C=	ENSP00000357280.1:p.Arg296=
ENST00000368298.2:n.393C=
ENST00000368299.7:c.1129C=	ENSP00000357282.3:p.Arg377=
ENST00000368300.8:c.1129C=	ENSP00000357283.4:p.Arg377=
ENST00000368301.6:c.1129C=	ENSP00000357284.2:p.Arg377=
ENST00000448611.6:c.793C=	ENSP00000395597.2:p.Arg265=
ENST00000473598.6:c.832C=	ENSP00000421821.1:p.Arg278=
ENST00000496738.5:n.514C=
ENST00000498722.2:n.361C=
ENST00000508500.1:c.7C=	ENSP00000424977.1:p.Arg3=
NM_001257374.2:c.793C=	NP_001244303.1:p.Arg265=
NM_001282624.1:c.886C=	NP_001269553.1:p.Arg296=
NM_001282625.1:c.1129C=	NP_001269554.1:p.Arg377=
NM_001282626.1:c.1129C=	NP_001269555.1:p.Arg377=
NM_005572.3:c.1129C= , LRG_254t1:c.1129C=	NP_005563.1:p.Arg377=
NM_170707.3:c.1129C=	NP_733821.1:p.Arg377=
NM_170708.3:c.1129C=	NP_733822.1:p.Arg377=
XM_011509533.1:c.793C=	XP_011507835.1:p.Arg265=
XM_011509534.1:c.505C=	XP_011507836.1:p.Arg169=
XR_921781.1:n.1418C=
XM_011509534.2:c.505C=	XP_011507836.1:p.Arg169=
XR_921781.2:n.1416C=
NM_170707.4:c.1129C= MANE Select	NP_733821.1:p.Arg377=
NM_001257374.3:c.793C=	NP_001244303.1:p.Arg265=
NM_001282626.2:c.1129C=	NP_001269555.1:p.Arg377=
NM_001282624.2:c.886C=	NP_001269553.1:p.Arg296=
NM_001282625.2:c.1129C=	NP_001269554.1:p.Arg377=
NM_005572.4:c.1129C= MANE Plus Clinical	NP_005563.1:p.Arg377=
NM_170708.4:c.1129C=	NP_733822.1:p.Arg377=