Canonical Allele Identifier: CA2648349271

Gene: LMNA

Linked Data

• gnomAD v4: 1-156136230-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156136231del , CM000663.2:g.156136231del	GRCh38
NC_000001.10:g.156106022del , CM000663.1:g.156106022del	GRCh37
NC_000001.9:g.154372646del	NCBI36
NG_008692.2:g.58659del , LRG_254:g.58659del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.617del	ENSP00000426535.3:p.Ser206ThrfsTer?
ENST00000498722.3:n.407del
ENST00000682650.1:c.1175del	ENSP00000506904.1:p.Ser392ThrfsTer?
ENST00000683032.1:c.1175del	ENSP00000506771.1:p.Ser392ThrfsTer?
ENST00000684195.1:c.1175del	ENSP00000508220.1:p.Ser392ThrfsTer?
ENST00000361308.9:c.1175del	ENSP00000355292.6:p.Ser392ThrfsTer?
ENST00000368300.9:c.1175del MANE Select	ENSP00000357283.4:p.Ser392ThrfsTer?
ENST00000496738.6:n.1550del
ENST00000674518.1:c.*525del	ENSP00000502261.1:n.*525del
ENST00000674600.1:c.*974del	ENSP00000501666.1:n.*974del
ENST00000674720.1:c.1175del	ENSP00000502798.1:p.Ser392ThrfsTer?
ENST00000675431.1:n.868del
ENST00000675455.1:c.*975del	ENSP00000501795.1:n.*975del
ENST00000675667.1:c.1175del	ENSP00000501803.1:p.Ser392ThrfsTer?
ENST00000675874.1:c.*646del	ENSP00000501851.1:n.*646del
ENST00000675881.1:c.*186del	ENSP00000501670.1:n.*186del
ENST00000675939.1:c.1175del	ENSP00000502256.1:p.Ser392ThrfsTer?
ENST00000675989.1:n.1550del
ENST00000676208.1:c.*278del	ENSP00000502468.1:n.*278del
ENST00000676283.1:n.1550del
ENST00000676385.2:c.1175del	ENSP00000502091.1:p.Ser392ThrfsTer?
ENST00000676434.1:c.*186del	ENSP00000501648.1:n.*186del
ENST00000677389.1:c.1175del MANE Plus Clinical	ENSP00000503633.1:p.Ser392ThrfsTer?
ENST00000347559.6:c.1175del	ENSP00000292304.3:p.Ser392ThrfsTer?
ENST00000361308.8:c.1175del	ENSP00000355292.5:p.Ser392ThrfsTer?
ENST00000368297.5:c.932del	ENSP00000357280.1:p.Ser311ThrfsTer?
ENST00000368298.2:n.439del
ENST00000368299.7:c.1175del	ENSP00000357282.3:p.Ser392ThrfsTer?
ENST00000368300.8:c.1175del	ENSP00000357283.4:p.Ser392ThrfsTer?
ENST00000368301.6:c.1175del	ENSP00000357284.2:p.Ser392ThrfsTer?
ENST00000448611.6:c.839del	ENSP00000395597.2:p.Ser280ThrfsTer?
ENST00000473598.6:c.878del	ENSP00000421821.1:p.Ser293ThrfsTer?
ENST00000496738.5:n.560del
ENST00000498722.2:n.407del
ENST00000508500.1:c.53del	ENSP00000424977.1:p.Ser18ThrfsTer?
NM_001257374.2:c.839del	NP_001244303.1:p.Ser280ThrfsTer?
NM_001282624.1:c.932del	NP_001269553.1:p.Ser311ThrfsTer?
NM_001282625.1:c.1175del	NP_001269554.1:p.Ser392ThrfsTer?
NM_001282626.1:c.1175del	NP_001269555.1:p.Ser392ThrfsTer?
NM_005572.3:c.1175del , LRG_254t1:c.1175del	NP_005563.1:p.Ser392ThrfsTer?
NM_170707.3:c.1175del	NP_733821.1:p.Ser392ThrfsTer?
NM_170708.3:c.1175del	NP_733822.1:p.Ser392ThrfsTer?
XM_011509533.1:c.839del	XP_011507835.1:p.Ser280ThrfsTer?
XM_011509534.1:c.551del	XP_011507836.1:p.Ser184ThrfsTer?
XR_921781.1:n.1464del
XM_011509534.2:c.551del	XP_011507836.1:p.Ser184ThrfsTer?
XR_921781.2:n.1462del
NM_170707.4:c.1175del MANE Select	NP_733821.1:p.Ser392ThrfsTer?
NM_001257374.3:c.839del	NP_001244303.1:p.Ser280ThrfsTer?
NM_001282626.2:c.1175del	NP_001269555.1:p.Ser392ThrfsTer?
NM_001282624.2:c.932del	NP_001269553.1:p.Ser311ThrfsTer?
NM_001282625.2:c.1175del	NP_001269554.1:p.Ser392ThrfsTer?
NM_005572.4:c.1175del MANE Plus Clinical	NP_005563.1:p.Ser392ThrfsTer?
NM_170708.4:c.1175del	NP_733822.1:p.Ser392ThrfsTer?