Canonical Allele Identifier: CA891842719

Gene: LMNA

Linked Data

• ClinVar Variation Id: 582185
• ClinVar RCV Id: RCV000706188
• dbSNP Id: rs1558133157
• MyVariant Identifiers: chr1:g.156106931del (hg19) ; chr1:g.156137140del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156137140del , CM000663.2:g.156137140del	GRCh38
NC_000001.10:g.156106931del , CM000663.1:g.156106931del	GRCh37
NC_000001.9:g.154373555del	NCBI36
NG_008692.2:g.59568del , LRG_254:g.59568del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.958del	ENSP00000426535.3:p.His320ThrfsTer?
ENST00000459904.2:n.764del
ENST00000498722.3:n.748del
ENST00000682650.1:c.1516del	ENSP00000506904.1:p.His506ThrfsTer?
ENST00000683032.1:c.1516del	ENSP00000506771.1:p.His506ThrfsTer?
ENST00000684195.1:c.1516del	ENSP00000508220.1:p.His506ThrfsTer?
ENST00000361308.9:c.1516del	ENSP00000355292.6:p.His506ThrfsTer?
ENST00000368300.9:c.1516del MANE Select	ENSP00000357283.4:p.His506ThrfsTer?
ENST00000496738.6:n.1975del
ENST00000674518.1:c.*866del	ENSP00000502261.1:n.*866del
ENST00000674600.1:c.*1315del	ENSP00000501666.1:n.*1315del
ENST00000674720.1:c.*78del	ENSP00000502798.1:n.*78del
ENST00000675431.1:n.1209del
ENST00000675455.1:c.*1316del	ENSP00000501795.1:n.*1316del
ENST00000675667.1:c.1516del	ENSP00000501803.1:p.His506ThrfsTer?
ENST00000675874.1:c.*987del	ENSP00000501851.1:n.*987del
ENST00000675881.1:c.*527del	ENSP00000501670.1:n.*527del
ENST00000675939.1:c.1516del	ENSP00000502256.1:p.His506ThrfsTer?
ENST00000675989.1:n.2375del
ENST00000676208.1:c.*619del	ENSP00000502468.1:n.*619del
ENST00000676283.1:n.1891del
ENST00000676385.2:c.1516del	ENSP00000502091.1:p.His506ThrfsTer?
ENST00000676434.1:c.*527del	ENSP00000501648.1:n.*527del
ENST00000677389.1:c.1516del MANE Plus Clinical	ENSP00000503633.1:p.His506ThrfsTer?
ENST00000347559.6:c.1516del	ENSP00000292304.3:p.His506ThrfsTer?
ENST00000361308.8:c.1312-51del	ENSP00000355292.5:n.1312-51del
ENST00000368297.5:c.1273del	ENSP00000357280.1:p.His425ThrfsTer?
ENST00000368298.2:n.1348del
ENST00000368299.7:c.1516del	ENSP00000357282.3:p.His506ThrfsTer?
ENST00000368300.8:c.1516del	ENSP00000357283.4:p.His506ThrfsTer?
ENST00000368301.6:c.1516del	ENSP00000357284.2:p.His506ThrfsTer?
ENST00000448611.6:c.1180del	ENSP00000395597.2:p.His394ThrfsTer?
ENST00000459904.1:n.764del
ENST00000473598.6:c.1219del	ENSP00000421821.1:p.His407ThrfsTer?
ENST00000496738.5:n.985del
ENST00000498722.2:n.748del
ENST00000508500.1:c.394del	ENSP00000424977.1:p.His132ThrfsTer?
NM_001257374.2:c.1180del	NP_001244303.1:p.His394ThrfsTer?
NM_001282624.1:c.1273del	NP_001269553.1:p.His425ThrfsTer?
NM_001282625.1:c.1516del	NP_001269554.1:p.His506ThrfsTer?
NM_001282626.1:c.1516del	NP_001269555.1:p.His506ThrfsTer?
NM_005572.3:c.1516del , LRG_254t1:c.1516del	NP_005563.1:p.His506ThrfsTer?
NM_170707.3:c.1516del	NP_733821.1:p.His506ThrfsTer?
NM_170708.3:c.1516del	NP_733822.1:p.His506ThrfsTer?
XM_011509533.1:c.1180del	XP_011507835.1:p.His394ThrfsTer?
XM_011509534.1:c.892del	XP_011507836.1:p.His298ThrfsTer?
XR_921781.1:n.1805del
XM_011509534.2:c.892del	XP_011507836.1:p.His298ThrfsTer?
XR_921781.2:n.1803del
NM_170707.4:c.1516del MANE Select	NP_733821.1:p.His506ThrfsTer?
NM_001257374.3:c.1180del	NP_001244303.1:p.His394ThrfsTer?
NM_001282626.2:c.1516del	NP_001269555.1:p.His506ThrfsTer?
NM_001282624.2:c.1273del	NP_001269553.1:p.His425ThrfsTer?
NM_001282625.2:c.1516del	NP_001269554.1:p.His506ThrfsTer?
NM_005572.4:c.1516del MANE Plus Clinical	NP_005563.1:p.His506ThrfsTer?
NM_170708.4:c.1516del	NP_733822.1:p.His506ThrfsTer?