Canonical Allele Identifier: CA1200472876

Gene: LMNA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156137114T= , CM000663.2:g.156137114T=	GRCh38
NC_000001.10:g.156106905T= , CM000663.1:g.156106905T=	GRCh37
NC_000001.9:g.154373529T=	NCBI36
NG_008692.2:g.59542T= , LRG_254:g.59542T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000504687.7:c.932T=	ENSP00000426535.3:p.Ile311=
ENST00000459904.2:n.738T=
ENST00000498722.3:n.722T=
ENST00000682650.1:c.1490T=	ENSP00000506904.1:p.Ile497=
ENST00000683032.1:c.1490T=	ENSP00000506771.1:p.Ile497=
ENST00000684195.1:c.1490T=	ENSP00000508220.1:p.Ile497=
ENST00000361308.9:c.1490T=	ENSP00000355292.6:p.Ile497=
ENST00000368300.9:c.1490T= MANE Select	ENSP00000357283.4:p.Ile497=
ENST00000496738.6:n.1949T=
ENST00000674518.1:c.*840T=	ENSP00000502261.1:n.*840T=
ENST00000674600.1:c.*1289T=	ENSP00000501666.1:n.*1289T=
ENST00000674720.1:c.*52T=	ENSP00000502798.1:n.*52T=
ENST00000675431.1:n.1183T=
ENST00000675455.1:c.*1290T=	ENSP00000501795.1:n.*1290T=
ENST00000675667.1:c.1490T=	ENSP00000501803.1:p.Ile497=
ENST00000675874.1:c.*961T=	ENSP00000501851.1:n.*961T=
ENST00000675881.1:c.*501T=	ENSP00000501670.1:n.*501T=
ENST00000675939.1:c.1490T=	ENSP00000502256.1:p.Ile497=
ENST00000675989.1:n.2349T=
ENST00000676208.1:c.*593T=	ENSP00000502468.1:n.*593T=
ENST00000676283.1:n.1865T=
ENST00000676385.2:c.1490T=	ENSP00000502091.1:p.Ile497=
ENST00000676434.1:c.*501T=	ENSP00000501648.1:n.*501T=
ENST00000677389.1:c.1490T= MANE Plus Clinical	ENSP00000503633.1:p.Ile497=
ENST00000347559.6:c.1490T=	ENSP00000292304.3:p.Ile497=
ENST00000361308.8:c.1312-77T=	ENSP00000355292.5:n.1312-77T=
ENST00000368297.5:c.1247T=	ENSP00000357280.1:p.Ile416=
ENST00000368298.2:n.1322T=
ENST00000368299.7:c.1490T=	ENSP00000357282.3:p.Ile497=
ENST00000368300.8:c.1490T=	ENSP00000357283.4:p.Ile497=
ENST00000368301.6:c.1490T=	ENSP00000357284.2:p.Ile497=
ENST00000448611.6:c.1154T=	ENSP00000395597.2:p.Ile385=
ENST00000459904.1:n.738T=
ENST00000473598.6:c.1193T=	ENSP00000421821.1:p.Ile398=
ENST00000496738.5:n.959T=
ENST00000498722.2:n.722T=
ENST00000508500.1:c.368T=	ENSP00000424977.1:p.Ile123=
NM_001257374.2:c.1154T=	NP_001244303.1:p.Ile385=
NM_001282624.1:c.1247T=	NP_001269553.1:p.Ile416=
NM_001282625.1:c.1490T=	NP_001269554.1:p.Ile497=
NM_001282626.1:c.1490T=	NP_001269555.1:p.Ile497=
NM_005572.3:c.1490T= , LRG_254t1:c.1490T=	NP_005563.1:p.Ile497=
NM_170707.3:c.1490T=	NP_733821.1:p.Ile497=
NM_170708.3:c.1490T=	NP_733822.1:p.Ile497=
XM_011509533.1:c.1154T=	XP_011507835.1:p.Ile385=
XM_011509534.1:c.866T=	XP_011507836.1:p.Ile289=
XR_921781.1:n.1779T=
XM_011509534.2:c.866T=	XP_011507836.1:p.Ile289=
XR_921781.2:n.1777T=
NM_170707.4:c.1490T= MANE Select	NP_733821.1:p.Ile497=
NM_001257374.3:c.1154T=	NP_001244303.1:p.Ile385=
NM_001282626.2:c.1490T=	NP_001269555.1:p.Ile497=
NM_001282624.2:c.1247T=	NP_001269553.1:p.Ile416=
NM_001282625.2:c.1490T=	NP_001269554.1:p.Ile497=
NM_005572.4:c.1490T= MANE Plus Clinical	NP_005563.1:p.Ile497=
NM_170708.4:c.1490T=	NP_733822.1:p.Ile497=