Canonical Allele Identifier: CA10576366

Gene: LMNA

Linked Data

• ClinVar Variation Id: 228272
• ClinVar RCV Id: RCV000223332
• dbSNP Id: rs876657650
• MyVariant Identifiers: chr1:g.156100527del (hg19) ; chr1:g.156130736del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156130736del , CM000663.2:g.156130736del	GRCh38
NC_000001.10:g.156100527del , CM000663.1:g.156100527del	GRCh37
NC_000001.9:g.154367151del	NCBI36
NG_008692.2:g.53164del , LRG_254:g.53164del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.-83del	ENSP00000426535.3:n.-83del
ENST00000682650.1:c.476del	ENSP00000506904.1:p.Glu159GlyfsTer18
ENST00000683032.1:c.476del	ENSP00000506771.1:p.Glu159GlyfsTer18
ENST00000684195.1:c.476del	ENSP00000508220.1:p.Glu159GlyfsTer18
ENST00000361308.9:c.476del	ENSP00000355292.6:p.Glu159GlyfsTer18
ENST00000368300.9:c.476del MANE Select	ENSP00000357283.4:p.Glu159GlyfsTer18
ENST00000496738.6:n.851del
ENST00000504687.6:c.-189del	ENSP00000426535.2:n.-189del
ENST00000674518.1:c.476del	ENSP00000502261.1:p.Glu159GlyfsTer18
ENST00000674600.1:c.*275del	ENSP00000501666.1:n.*275del
ENST00000674720.1:c.476del	ENSP00000502798.1:p.Glu159GlyfsTer18
ENST00000675431.1:n.169del
ENST00000675455.1:c.*276del	ENSP00000501795.1:n.*276del
ENST00000675667.1:c.476del	ENSP00000501803.1:p.Glu159GlyfsTer18
ENST00000675874.1:c.357-3667del	ENSP00000501851.1:n.357-3667del
ENST00000675881.1:c.476del	ENSP00000501670.1:p.Glu159GlyfsTer18
ENST00000675939.1:c.476del	ENSP00000502256.1:p.Glu159GlyfsTer18
ENST00000675989.1:n.851del
ENST00000676208.1:c.476del	ENSP00000502468.1:p.Glu159GlyfsTer18
ENST00000676283.1:n.851del
ENST00000676385.2:c.476del	ENSP00000502091.1:p.Glu159GlyfsTer18
ENST00000676434.1:c.476del	ENSP00000501648.1:p.Glu159GlyfsTer18
ENST00000677389.1:c.476del MANE Plus Clinical	ENSP00000503633.1:p.Glu159GlyfsTer18
ENST00000347559.6:c.476del	ENSP00000292304.3:p.Glu159GlyfsTer18
ENST00000361308.8:c.476del	ENSP00000355292.5:p.Glu159GlyfsTer18
ENST00000368297.5:c.233del	ENSP00000357280.1:p.Glu78GlyfsTer18
ENST00000368299.7:c.476del	ENSP00000357282.3:p.Glu159GlyfsTer18
ENST00000368300.8:c.476del	ENSP00000357283.4:p.Glu159GlyfsTer18
ENST00000368301.6:c.476del	ENSP00000357284.2:p.Glu159GlyfsTer18
ENST00000448611.6:c.140del	ENSP00000395597.2:p.Glu47GlyfsTer18
ENST00000469565.6:n.510del
ENST00000470199.2:n.418del
ENST00000473598.6:c.179del	ENSP00000421821.1:p.Glu60GlyfsTer18
ENST00000502357.5:n.374del
ENST00000502751.5:n.448del
ENST00000504687.5:c.227del	ENSP00000426535.1:p.Glu76GlyfsTer18
ENST00000515459.5:c.*150del	ENSP00000424518.1:n.*150del
NM_001257374.2:c.140del	NP_001244303.1:p.Glu47GlyfsTer18
NM_001282624.1:c.233del	NP_001269553.1:p.Glu78GlyfsTer18
NM_001282625.1:c.476del	NP_001269554.1:p.Glu159GlyfsTer18
NM_001282626.1:c.476del	NP_001269555.1:p.Glu159GlyfsTer18
NM_005572.3:c.476del , LRG_254t1:c.476del	NP_005563.1:p.Glu159GlyfsTer18
NM_170707.3:c.476del	NP_733821.1:p.Glu159GlyfsTer18
NM_170708.3:c.476del	NP_733822.1:p.Glu159GlyfsTer18
XM_011509533.1:c.140del	XP_011507835.1:p.Glu47GlyfsTer18
XM_011509534.1:c.-189del	XP_011507836.1:n.-189del
XR_921781.1:n.725del
XM_011509534.2:c.-189del	XP_011507836.1:n.-189del
XR_921781.2:n.723del
NM_170707.4:c.476del MANE Select	NP_733821.1:p.Glu159GlyfsTer18
NM_001257374.3:c.140del	NP_001244303.1:p.Glu47GlyfsTer18
NM_001282626.2:c.476del	NP_001269555.1:p.Glu159GlyfsTer18
NM_001282624.2:c.233del	NP_001269553.1:p.Glu78GlyfsTer18
NM_001282625.2:c.476del	NP_001269554.1:p.Glu159GlyfsTer18
NM_005572.4:c.476del MANE Plus Clinical	NP_005563.1:p.Glu159GlyfsTer18
NM_170708.4:c.476del	NP_733822.1:p.Glu159GlyfsTer18