Canonical Allele Identifier: CA1143538357
Gene: LMNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156136065_156136094delinsGGCCCTGGACATGGAGATCCACGCCTACCG , CM000663.2:g.156136065_156136094delinsGGCCCTGGACATGGAGATCCACGCCTACCG GRCh38
NC_000001.10:g.156105856_156105885delinsGGCCCTGGACATGGAGATCCACGCCTACCG , CM000663.1:g.156105856_156105885delinsGGCCCTGGACATGGAGATCCACGCCTACCG GRCh37
NC_000001.9:g.154372480_154372509delinsGGCCCTGGACATGGAGATCCACGCCTACCG NCBI36
NG_008692.2:g.58493_58522delinsGGCCCTGGACATGGAGATCCACGCCTACCG , LRG_254:g.58493_58522delinsGGCCCTGGACATGGAGATCCACGCCTACCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000504687.7:c.543_572delinsGGCCCTGGACATGGAGATCCACGCCTACCG ENSP00000426535.3:p.Leu181=
ENST00000498722.3:n.333_362delinsGGCCCTGGACATGGAGATCCACGCCTACCG
ENST00000682650.1:c.1101_1130delinsGGCCCTGGACATGGAGATCCACGCCTACCG ENSP00000506904.1:p.Leu367=
ENST00000683032.1:c.1101_1130delinsGGCCCTGGACATGGAGATCCACGCCTACCG ENSP00000506771.1:p.Leu367=
ENST00000684195.1:c.1101_1130delinsGGCCCTGGACATGGAGATCCACGCCTACCG ENSP00000508220.1:p.Leu367=
ENST00000361308.9:c.1101_1130delinsGGCCCTGGACATGGAGATCCACGCCTACCG ENSP00000355292.6:p.Leu367=
ENST00000368300.9:c.1101_1130delinsGGCCCTGGACATGGAGATCCACGCCTACCG MANE Select ENSP00000357283.4:p.Leu367=
ENST00000496738.6:n.1476_1505delinsGGCCCTGGACATGGAGATCCACGCCTACCG
ENST00000674518.1:c.*451_*480delinsGGCCCTGGACATGGAGATCCACGCCTACCG ENSP00000502261.1:n.*451_*480delinsGGCCCTGGACATGGAGATCCACGCCT...
ENST00000674600.1:c.*900_*929delinsGGCCCTGGACATGGAGATCCACGCCTACCG ENSP00000501666.1:n.*900_*929delinsGGCCCTGGACATGGAGATCCACGCCT...
ENST00000674720.1:c.1101_1130delinsGGCCCTGGACATGGAGATCCACGCCTACCG ENSP00000502798.1:p.Leu367=
ENST00000675431.1:n.794_823delinsGGCCCTGGACATGGAGATCCACGCCTACCG
ENST00000675455.1:c.*901_*930delinsGGCCCTGGACATGGAGATCCACGCCTACCG ENSP00000501795.1:n.*901_*930delinsGGCCCTGGACATGGAGATCCACGCCT...
ENST00000675667.1:c.1101_1130delinsGGCCCTGGACATGGAGATCCACGCCTACCG ENSP00000501803.1:p.Leu367=
ENST00000675874.1:c.*572_*601delinsGGCCCTGGACATGGAGATCCACGCCTACCG ENSP00000501851.1:n.*572_*601delinsGGCCCTGGACATGGAGATCCACGCCT...
ENST00000675881.1:c.*112_*141delinsGGCCCTGGACATGGAGATCCACGCCTACCG ENSP00000501670.1:n.*112_*141delinsGGCCCTGGACATGGAGATCCACGCCT...
ENST00000675939.1:c.1101_1130delinsGGCCCTGGACATGGAGATCCACGCCTACCG ENSP00000502256.1:p.Leu367=
ENST00000675989.1:n.1476_1505delinsGGCCCTGGACATGGAGATCCACGCCTACCG
ENST00000676208.1:c.*112_*141delinsGGCCCTGGACATGGAGATCCACGCCTACCG ENSP00000502468.1:n.*112_*141delinsGGCCCTGGACATGGAGATCCACGCCT...
ENST00000676283.1:n.1476_1505delinsGGCCCTGGACATGGAGATCCACGCCTACCG
ENST00000676385.2:c.1101_1130delinsGGCCCTGGACATGGAGATCCACGCCTACCG ENSP00000502091.1:p.Leu367=
ENST00000676434.1:c.*112_*141delinsGGCCCTGGACATGGAGATCCACGCCTACCG ENSP00000501648.1:n.*112_*141delinsGGCCCTGGACATGGAGATCCACGCCT...
ENST00000677389.1:c.1101_1130delinsGGCCCTGGACATGGAGATCCACGCCTACCG MANE Plus Clinical ENSP00000503633.1:p.Leu367=
ENST00000347559.6:c.1101_1130delinsGGCCCTGGACATGGAGATCCACGCCTACCG ENSP00000292304.3:p.Leu367=
ENST00000361308.8:c.1101_1130delinsGGCCCTGGACATGGAGATCCACGCCTACCG ENSP00000355292.5:p.Leu367=
ENST00000368297.5:c.858_887delinsGGCCCTGGACATGGAGATCCACGCCTACCG ENSP00000357280.1:p.Leu286=
ENST00000368298.2:n.365_394delinsGGCCCTGGACATGGAGATCCACGCCTACCG
ENST00000368299.7:c.1101_1130delinsGGCCCTGGACATGGAGATCCACGCCTACCG ENSP00000357282.3:p.Leu367=
ENST00000368300.8:c.1101_1130delinsGGCCCTGGACATGGAGATCCACGCCTACCG ENSP00000357283.4:p.Leu367=
ENST00000368301.6:c.1101_1130delinsGGCCCTGGACATGGAGATCCACGCCTACCG ENSP00000357284.2:p.Leu367=
ENST00000448611.6:c.765_794delinsGGCCCTGGACATGGAGATCCACGCCTACCG ENSP00000395597.2:p.Leu255=
ENST00000473598.6:c.804_833delinsGGCCCTGGACATGGAGATCCACGCCTACCG ENSP00000421821.1:p.Leu268=
ENST00000496738.5:n.486_515delinsGGCCCTGGACATGGAGATCCACGCCTACCG
ENST00000498722.2:n.333_362delinsGGCCCTGGACATGGAGATCCACGCCTACCG
NM_001257374.2:c.765_794delinsGGCCCTGGACATGGAGATCCACGCCTACCG NP_001244303.1:p.Leu255=
NM_001282624.1:c.858_887delinsGGCCCTGGACATGGAGATCCACGCCTACCG NP_001269553.1:p.Leu286=
NM_001282625.1:c.1101_1130delinsGGCCCTGGACATGGAGATCCACGCCTACCG NP_001269554.1:p.Leu367=
NM_001282626.1:c.1101_1130delinsGGCCCTGGACATGGAGATCCACGCCTACCG NP_001269555.1:p.Leu367=
NM_005572.3:c.1101_1130delinsGGCCCTGGACATGGAGATCCACGCCTACCG , LRG_254t1:c.1101_1130delinsGGCCCTGGACATGGAGATCCACGCCTACCG NP_005563.1:p.Leu367=
NM_170707.3:c.1101_1130delinsGGCCCTGGACATGGAGATCCACGCCTACCG NP_733821.1:p.Leu367=
NM_170708.3:c.1101_1130delinsGGCCCTGGACATGGAGATCCACGCCTACCG NP_733822.1:p.Leu367=
XM_011509533.1:c.765_794delinsGGCCCTGGACATGGAGATCCACGCCTACCG XP_011507835.1:p.Leu255=
XM_011509534.1:c.477_506delinsGGCCCTGGACATGGAGATCCACGCCTACCG XP_011507836.1:p.Leu159=
XR_921781.1:n.1390_1419delinsGGCCCTGGACATGGAGATCCACGCCTACCG
XM_011509534.2:c.477_506delinsGGCCCTGGACATGGAGATCCACGCCTACCG XP_011507836.1:p.Leu159=
XR_921781.2:n.1388_1417delinsGGCCCTGGACATGGAGATCCACGCCTACCG
NM_170707.4:c.1101_1130delinsGGCCCTGGACATGGAGATCCACGCCTACCG MANE Select NP_733821.1:p.Leu367=
NM_001257374.3:c.765_794delinsGGCCCTGGACATGGAGATCCACGCCTACCG NP_001244303.1:p.Leu255=
NM_001282626.2:c.1101_1130delinsGGCCCTGGACATGGAGATCCACGCCTACCG NP_001269555.1:p.Leu367=
NM_001282624.2:c.858_887delinsGGCCCTGGACATGGAGATCCACGCCTACCG NP_001269553.1:p.Leu286=
NM_001282625.2:c.1101_1130delinsGGCCCTGGACATGGAGATCCACGCCTACCG NP_001269554.1:p.Leu367=
NM_005572.4:c.1101_1130delinsGGCCCTGGACATGGAGATCCACGCCTACCG MANE Plus Clinical NP_005563.1:p.Leu367=
NM_170708.4:c.1101_1130delinsGGCCCTGGACATGGAGATCCACGCCTACCG NP_733822.1:p.Leu367=