Canonical Allele Identifier: CA1200467785

Gene: LMNA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156130735_156130736delinsGA , CM000663.2:g.156130735_156130736delinsGA	GRCh38
NC_000001.10:g.156100526_156100527delinsGA , CM000663.1:g.156100526_156100527delinsGA	GRCh37
NC_000001.9:g.154367150_154367151delinsGA	NCBI36
NG_008692.2:g.53163_53164delinsGA , LRG_254:g.53163_53164delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.-84_-83delinsGA	ENSP00000426535.3:n.-84_-83delinsGA
ENST00000682650.1:c.475_476delinsGA	ENSP00000506904.1:p.Glu159=
ENST00000683032.1:c.475_476delinsGA	ENSP00000506771.1:p.Glu159=
ENST00000684195.1:c.475_476delinsGA	ENSP00000508220.1:p.Glu159=
ENST00000361308.9:c.475_476delinsGA	ENSP00000355292.6:p.Glu159=
ENST00000368300.9:c.475_476delinsGA MANE Select	ENSP00000357283.4:p.Glu159=
ENST00000496738.6:n.850_851delinsGA
ENST00000504687.6:c.-190_-189delinsGA	ENSP00000426535.2:n.-190_-189delinsGA
ENST00000674518.1:c.475_476delinsGA	ENSP00000502261.1:p.Glu159=
ENST00000674600.1:c.*274_*275delinsGA	ENSP00000501666.1:n.*274_*275delinsGA
ENST00000674720.1:c.475_476delinsGA	ENSP00000502798.1:p.Glu159=
ENST00000675431.1:n.168_169delinsGA
ENST00000675455.1:c.*275_*276delinsGA	ENSP00000501795.1:n.*275_*276delinsGA
ENST00000675667.1:c.475_476delinsGA	ENSP00000501803.1:p.Glu159=
ENST00000675874.1:c.357-3668_357-3667delinsGA	ENSP00000501851.1:n.357-3668_357-3667delinsGA
ENST00000675881.1:c.475_476delinsGA	ENSP00000501670.1:p.Glu159=
ENST00000675939.1:c.475_476delinsGA	ENSP00000502256.1:p.Glu159=
ENST00000675989.1:n.850_851delinsGA
ENST00000676208.1:c.475_476delinsGA	ENSP00000502468.1:p.Glu159=
ENST00000676283.1:n.850_851delinsGA
ENST00000676385.2:c.475_476delinsGA	ENSP00000502091.1:p.Glu159=
ENST00000676434.1:c.475_476delinsGA	ENSP00000501648.1:p.Glu159=
ENST00000677389.1:c.475_476delinsGA MANE Plus Clinical	ENSP00000503633.1:p.Glu159=
ENST00000347559.6:c.475_476delinsGA	ENSP00000292304.3:p.Glu159=
ENST00000361308.8:c.475_476delinsGA	ENSP00000355292.5:p.Glu159=
ENST00000368297.5:c.232_233delinsGA	ENSP00000357280.1:p.Glu78=
ENST00000368299.7:c.475_476delinsGA	ENSP00000357282.3:p.Glu159=
ENST00000368300.8:c.475_476delinsGA	ENSP00000357283.4:p.Glu159=
ENST00000368301.6:c.475_476delinsGA	ENSP00000357284.2:p.Glu159=
ENST00000448611.6:c.139_140delinsGA	ENSP00000395597.2:p.Glu47=
ENST00000469565.6:n.509_510delinsGA
ENST00000470199.2:n.417_418delinsGA
ENST00000473598.6:c.178_179delinsGA	ENSP00000421821.1:p.Glu60=
ENST00000502357.5:n.373_374delinsGA
ENST00000502751.5:n.447_448delinsGA
ENST00000504687.5:c.226_227delinsGA	ENSP00000426535.1:p.Glu76=
ENST00000515459.5:c.*149_*150delinsGA	ENSP00000424518.1:n.*149_*150delinsGA
NM_001257374.2:c.139_140delinsGA	NP_001244303.1:p.Glu47=
NM_001282624.1:c.232_233delinsGA	NP_001269553.1:p.Glu78=
NM_001282625.1:c.475_476delinsGA	NP_001269554.1:p.Glu159=
NM_001282626.1:c.475_476delinsGA	NP_001269555.1:p.Glu159=
NM_005572.3:c.475_476delinsGA , LRG_254t1:c.475_476delinsGA	NP_005563.1:p.Glu159=
NM_170707.3:c.475_476delinsGA	NP_733821.1:p.Glu159=
NM_170708.3:c.475_476delinsGA	NP_733822.1:p.Glu159=
XM_011509533.1:c.139_140delinsGA	XP_011507835.1:p.Glu47=
XM_011509534.1:c.-190_-189delinsGA	XP_011507836.1:n.-190_-189delinsGA
XR_921781.1:n.724_725delinsGA
XM_011509534.2:c.-190_-189delinsGA	XP_011507836.1:n.-190_-189delinsGA
XR_921781.2:n.722_723delinsGA
NM_170707.4:c.475_476delinsGA MANE Select	NP_733821.1:p.Glu159=
NM_001257374.3:c.139_140delinsGA	NP_001244303.1:p.Glu47=
NM_001282626.2:c.475_476delinsGA	NP_001269555.1:p.Glu159=
NM_001282624.2:c.232_233delinsGA	NP_001269553.1:p.Glu78=
NM_001282625.2:c.475_476delinsGA	NP_001269554.1:p.Glu159=
NM_005572.4:c.475_476delinsGA MANE Plus Clinical	NP_005563.1:p.Glu159=
NM_170708.4:c.475_476delinsGA	NP_733822.1:p.Glu159=