Canonical Allele Identifier: CA018329

Gene: LMNA

Linked Data

• ClinVar Variation Id: 66919
• ClinVar RCV Id: RCV000057434
• dbSNP Id: rs62636507
• MyVariant Identifiers: chr1:g.156104305del (hg19) ; chr1:g.156134514del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156134515del , CM000663.2:g.156134515del	GRCh38
NC_000001.10:g.156104306del , CM000663.1:g.156104306del	GRCh37
NC_000001.9:g.154370930del	NCBI36
NG_008692.2:g.56943del , LRG_254:g.56943del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.68del	ENSP00000426535.3:p.Asn23ThrfsTer?
ENST00000682650.1:c.626del	ENSP00000506904.1:p.Asn209ThrfsTer?
ENST00000683032.1:c.626del	ENSP00000506771.1:p.Asn209ThrfsTer?
ENST00000684195.1:c.626del	ENSP00000508220.1:p.Asn209ThrfsTer?
ENST00000361308.9:c.626del	ENSP00000355292.6:p.Asn209ThrfsTer?
ENST00000368300.9:c.626del MANE Select	ENSP00000357283.4:p.Asn209ThrfsTer?
ENST00000496738.6:n.1001del
ENST00000504687.6:c.-39del	ENSP00000426535.2:n.-39del
ENST00000674518.1:c.626del	ENSP00000502261.1:p.Asn209ThrfsTer?
ENST00000674600.1:c.*425del	ENSP00000501666.1:n.*425del
ENST00000674720.1:c.626del	ENSP00000502798.1:p.Asn209ThrfsTer?
ENST00000675431.1:n.319del
ENST00000675455.1:c.*426del	ENSP00000501795.1:n.*426del
ENST00000675667.1:c.626del	ENSP00000501803.1:p.Asn209ThrfsTer?
ENST00000675874.1:c.*97del	ENSP00000501851.1:n.*97del
ENST00000675881.1:c.626del	ENSP00000501670.1:p.Asn209ThrfsTer?
ENST00000675939.1:c.626del	ENSP00000502256.1:p.Asn209ThrfsTer?
ENST00000675989.1:n.1001del
ENST00000676208.1:c.626del	ENSP00000502468.1:p.Asn209ThrfsTer?
ENST00000676283.1:n.1001del
ENST00000676385.2:c.626del	ENSP00000502091.1:p.Asn209ThrfsTer?
ENST00000676434.1:c.626del	ENSP00000501648.1:p.Asn209ThrfsTer?
ENST00000677389.1:c.626del MANE Plus Clinical	ENSP00000503633.1:p.Asn209ThrfsTer?
ENST00000347559.6:c.626del	ENSP00000292304.3:p.Asn209ThrfsTer?
ENST00000361308.8:c.626del	ENSP00000355292.5:p.Asn209ThrfsTer?
ENST00000368297.5:c.383del	ENSP00000357280.1:p.Asn128ThrfsTer?
ENST00000368299.7:c.626del	ENSP00000357282.3:p.Asn209ThrfsTer?
ENST00000368300.8:c.626del	ENSP00000357283.4:p.Asn209ThrfsTer?
ENST00000368301.6:c.626del	ENSP00000357284.2:p.Asn209ThrfsTer?
ENST00000448611.6:c.290del	ENSP00000395597.2:p.Asn97ThrfsTer?
ENST00000473598.6:c.329del	ENSP00000421821.1:p.Asn110ThrfsTer?
ENST00000502357.5:n.524del
ENST00000504687.5:c.377del	ENSP00000426535.1:p.Asn126ThrfsTer?
ENST00000515459.5:c.*300del	ENSP00000424518.1:n.*300del
NM_001257374.2:c.290del	NP_001244303.1:p.Asn97ThrfsTer?
NM_001282624.1:c.383del	NP_001269553.1:p.Asn128ThrfsTer?
NM_001282625.1:c.626del	NP_001269554.1:p.Asn209ThrfsTer?
NM_001282626.1:c.626del	NP_001269555.1:p.Asn209ThrfsTer?
NM_005572.3:c.626del , LRG_254t1:c.626del	NP_005563.1:p.Asn209ThrfsTer?
NM_170707.3:c.626del	NP_733821.1:p.Asn209ThrfsTer?
NM_170708.3:c.626del	NP_733822.1:p.Asn209ThrfsTer?
XM_011509533.1:c.290del	XP_011507835.1:p.Asn97ThrfsTer?
XM_011509534.1:c.-39del	XP_011507836.1:n.-39del
XR_921781.1:n.875del
XM_011509534.2:c.-39del	XP_011507836.1:n.-39del
XR_921781.2:n.873del
NM_170707.4:c.626del MANE Select	NP_733821.1:p.Asn209ThrfsTer?
NM_001257374.3:c.290del	NP_001244303.1:p.Asn97ThrfsTer?
NM_001282626.2:c.626del	NP_001269555.1:p.Asn209ThrfsTer?
NM_001282624.2:c.383del	NP_001269553.1:p.Asn128ThrfsTer?
NM_001282625.2:c.626del	NP_001269554.1:p.Asn209ThrfsTer?
NM_005572.4:c.626del MANE Plus Clinical	NP_005563.1:p.Asn209ThrfsTer?
NM_170708.4:c.626del	NP_733822.1:p.Asn209ThrfsTer?