Canonical Allele Identifier: CA018901

Gene: LMNA

Linked Data

• ClinVar Variation Id: 14491
• ClinVar RCV Id: RCV000015581 ; RCV000057492 ; RCV000681609
• dbSNP Id: rs56771886
• MyVariant Identifiers: chr1:g.156105714del (hg19) ; chr1:g.156135923del (hg38)
• PubMed: PMID:10662742 ; PMID:20301717

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156135924del , CM000663.2:g.156135924del	GRCh38
NC_000001.10:g.156105715del , CM000663.1:g.156105715del	GRCh37
NC_000001.9:g.154372339del	NCBI36
NG_008692.2:g.58352del , LRG_254:g.58352del

Transcript Alleles

HGVS	Amino-acid change
ENST00000504687.7:c.402del	ENSP00000426535.3:p.Arg135GlufsTer?
ENST00000498722.3:n.192del
ENST00000682650.1:c.960del	ENSP00000506904.1:p.Arg321GlufsTer?
ENST00000683032.1:c.960del	ENSP00000506771.1:p.Arg321GlufsTer?
ENST00000684195.1:c.960del	ENSP00000508220.1:p.Arg321GlufsTer?
ENST00000361308.9:c.960del	ENSP00000355292.6:p.Arg321GlufsTer?
ENST00000368300.9:c.960del MANE Select	ENSP00000357283.4:p.Arg321GlufsTer?
ENST00000496738.6:n.1335del
ENST00000674518.1:c.*310del	ENSP00000502261.1:n.*310del
ENST00000674600.1:c.*759del	ENSP00000501666.1:n.*759del
ENST00000674720.1:c.960del	ENSP00000502798.1:p.Arg321GlufsTer?
ENST00000675431.1:n.653del
ENST00000675455.1:c.*760del	ENSP00000501795.1:n.*760del
ENST00000675667.1:c.960del	ENSP00000501803.1:p.Arg321GlufsTer?
ENST00000675874.1:c.*431del	ENSP00000501851.1:n.*431del
ENST00000675881.1:c.1000del	ENSP00000501670.1:p.Ser334ArgfsTer?
ENST00000675939.1:c.960del	ENSP00000502256.1:p.Arg321GlufsTer?
ENST00000675989.1:n.1335del
ENST00000676208.1:c.1000del	ENSP00000502468.1:p.Ser334ArgfsTer?
ENST00000676283.1:n.1335del
ENST00000676385.2:c.960del	ENSP00000502091.1:p.Arg321GlufsTer?
ENST00000676434.1:c.1000del	ENSP00000501648.1:p.Ser334ArgfsTer?
ENST00000677389.1:c.960del MANE Plus Clinical	ENSP00000503633.1:p.Arg321GlufsTer?
ENST00000347559.6:c.960del	ENSP00000292304.3:p.Arg321GlufsTer?
ENST00000361308.8:c.960del	ENSP00000355292.5:p.Arg321GlufsTer?
ENST00000368297.5:c.717del	ENSP00000357280.1:p.Arg240GlufsTer?
ENST00000368298.2:n.224del
ENST00000368299.7:c.960del	ENSP00000357282.3:p.Arg321GlufsTer?
ENST00000368300.8:c.960del	ENSP00000357283.4:p.Arg321GlufsTer?
ENST00000368301.6:c.960del	ENSP00000357284.2:p.Arg321GlufsTer?
ENST00000448611.6:c.624del	ENSP00000395597.2:p.Arg209GlufsTer?
ENST00000473598.6:c.663del	ENSP00000421821.1:p.Arg222GlufsTer?
ENST00000496738.5:n.345del
ENST00000498722.2:n.192del
NM_001257374.2:c.624del	NP_001244303.1:p.Arg209GlufsTer?
NM_001282624.1:c.717del	NP_001269553.1:p.Arg240GlufsTer?
NM_001282625.1:c.960del	NP_001269554.1:p.Arg321GlufsTer?
NM_001282626.1:c.960del	NP_001269555.1:p.Arg321GlufsTer?
NM_005572.3:c.960del , LRG_254t1:c.960del	NP_005563.1:p.Arg321GlufsTer?
NM_170707.3:c.960del	NP_733821.1:p.Arg321GlufsTer?
NM_170708.3:c.960del	NP_733822.1:p.Arg321GlufsTer?
XM_011509533.1:c.624del	XP_011507835.1:p.Arg209GlufsTer?
XM_011509534.1:c.336del	XP_011507836.1:p.Arg113GlufsTer?
XR_921781.1:n.1249del
XM_011509534.2:c.336del	XP_011507836.1:p.Arg113GlufsTer?
XR_921781.2:n.1247del
NM_170707.4:c.960del MANE Select	NP_733821.1:p.Arg321GlufsTer?
NM_001257374.3:c.624del	NP_001244303.1:p.Arg209GlufsTer?
NM_001282626.2:c.960del	NP_001269555.1:p.Arg321GlufsTer?
NM_001282624.2:c.717del	NP_001269553.1:p.Arg240GlufsTer?
NM_001282625.2:c.960del	NP_001269554.1:p.Arg321GlufsTer?
NM_005572.4:c.960del MANE Plus Clinical	NP_005563.1:p.Arg321GlufsTer?
NM_170708.4:c.960del	NP_733822.1:p.Arg321GlufsTer?