Canonical Allele Identifier: CA2586964332

Gene: LMNA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156138756del , CM000663.2:g.156138756del	GRCh38
NC_000001.10:g.156108547del , CM000663.1:g.156108547del	GRCh37
NC_000001.9:g.154375171del	NCBI36
NG_008692.2:g.61184del , LRG_254:g.61184del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.1409del	ENSP00000426535.3:p.Gln470ArgfsTer?
ENST00000682650.1:c.1877del	ENSP00000506904.1:p.Gln626ArgfsTer?
ENST00000683032.1:c.1967del	ENSP00000506771.1:p.Gln656ArgfsTer?
ENST00000683773.1:n.163+149del
ENST00000684195.1:c.*1059del	ENSP00000508220.1:n.*1059del
ENST00000361308.9:c.1967del	ENSP00000355292.6:p.Gln656ArgfsTer?
ENST00000368300.9:c.1967del MANE Select	ENSP00000357283.4:p.Gln656ArgfsTer?
ENST00000674518.1:c.*1317del	ENSP00000502261.1:n.*1317del
ENST00000674600.1:c.*1766del	ENSP00000501666.1:n.*1766del
ENST00000675455.1:c.*1767del	ENSP00000501795.1:n.*1767del
ENST00000675667.1:c.1967del	ENSP00000501803.1:p.Gln656ArgfsTer2
ENST00000675874.1:c.*1438del	ENSP00000501851.1:n.*1438del
ENST00000675881.1:c.*978del	ENSP00000501670.1:n.*978del
ENST00000675939.1:c.1967del	ENSP00000502256.1:p.Gln656ArgfsTer?
ENST00000675989.1:n.3570del
ENST00000676208.1:c.*1070del	ENSP00000502468.1:n.*1070del
ENST00000676385.2:c.1877del	ENSP00000502091.1:p.Gln626ArgfsTer?
ENST00000676434.1:c.*1722del	ENSP00000501648.1:n.*1722del
ENST00000347559.6:c.1877del	ENSP00000292304.3:p.Gln626ArgfsTer?
ENST00000368299.7:c.1818+149del	ENSP00000357282.3:n.1818+149del
ENST00000368300.8:c.1967del	ENSP00000357283.4:p.Gln656ArgfsTer?
ENST00000448611.6:c.1631del	ENSP00000395597.2:p.Gln544ArgfsTer14
ENST00000473598.6:c.1670del	ENSP00000421821.1:p.Gln557ArgfsTer?
ENST00000496738.5:n.2180del
ENST00000506981.1:n.551del
ENST00000508500.1:c.755del	ENSP00000424977.1:p.Gln252ArgfsTer?
NM_001257374.2:c.1631del	NP_001244303.1:p.Gln544ArgfsTer14
NM_001282626.1:c.1818+149del	NP_001269555.1:n.1818+149del
NM_170707.3:c.1967del	NP_733821.1:p.Gln656ArgfsTer?
NM_170708.3:c.1877del	NP_733822.1:p.Gln626ArgfsTer?
XM_011509533.1:c.1631del	XP_011507835.1:p.Gln544ArgfsTer?
XM_011509534.1:c.1343del	XP_011507836.1:p.Gln448ArgfsTer?
XR_921781.1:n.2256del
XM_011509534.2:c.1343del	XP_011507836.1:p.Gln448ArgfsTer?
XR_921781.2:n.2254del
NM_170707.4:c.1967del MANE Select	NP_733821.1:p.Gln656ArgfsTer?
NM_001257374.3:c.1631del	NP_001244303.1:p.Gln544ArgfsTer14
NM_001282626.2:c.1818+149del	NP_001269555.1:n.1818+149del
NM_170708.4:c.1877del	NP_733822.1:p.Gln626ArgfsTer?