Canonical Allele Identifier: CA1200467744
Gene: LMNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156130723_156130738delinsAAGCGCACGCTGGAGG , CM000663.2:g.156130723_156130738delinsAAGCGCACGCTGGAGG GRCh38
NC_000001.10:g.156100514_156100529delinsAAGCGCACGCTGGAGG , CM000663.1:g.156100514_156100529delinsAAGCGCACGCTGGAGG GRCh37
NC_000001.9:g.154367138_154367153delinsAAGCGCACGCTGGAGG NCBI36
NG_008692.2:g.53151_53166delinsAAGCGCACGCTGGAGG , LRG_254:g.53151_53166delinsAAGCGCACGCTGGAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000504687.7:c.-96_-81delinsAAGCGCACGCTGGAGG ENSP00000426535.3:n.-96_-81delinsAAGCGCACGCTGGAGG
ENST00000682650.1:c.463_478delinsAAGCGCACGCTGGAGG ENSP00000506904.1:p.Lys155=
ENST00000683032.1:c.463_478delinsAAGCGCACGCTGGAGG ENSP00000506771.1:p.Lys155=
ENST00000684195.1:c.463_478delinsAAGCGCACGCTGGAGG ENSP00000508220.1:p.Lys155=
ENST00000361308.9:c.463_478delinsAAGCGCACGCTGGAGG ENSP00000355292.6:p.Lys155=
ENST00000368300.9:c.463_478delinsAAGCGCACGCTGGAGG MANE Select ENSP00000357283.4:p.Lys155=
ENST00000496738.6:n.838_853delinsAAGCGCACGCTGGAGG
ENST00000504687.6:c.-202_-187delinsAAGCGCACGCTGGAGG ENSP00000426535.2:n.-202_-187delinsAAGCGCACGCTGGAGG
ENST00000674518.1:c.463_478delinsAAGCGCACGCTGGAGG ENSP00000502261.1:p.Lys155=
ENST00000674600.1:c.*262_*277delinsAAGCGCACGCTGGAGG ENSP00000501666.1:n.*262_*277delinsAAGCGCACGCTGGAGG
ENST00000674720.1:c.463_478delinsAAGCGCACGCTGGAGG ENSP00000502798.1:p.Lys155=
ENST00000675431.1:n.156_171delinsAAGCGCACGCTGGAGG
ENST00000675455.1:c.*263_*278delinsAAGCGCACGCTGGAGG ENSP00000501795.1:n.*263_*278delinsAAGCGCACGCTGGAGG
ENST00000675667.1:c.463_478delinsAAGCGCACGCTGGAGG ENSP00000501803.1:p.Lys155=
ENST00000675874.1:c.357-3680_357-3665delinsAAGCGCACGCTGGAGG ENSP00000501851.1:n.357-3680_357-3665delinsAAGCGCACGCTGGAGG
ENST00000675881.1:c.463_478delinsAAGCGCACGCTGGAGG ENSP00000501670.1:p.Lys155=
ENST00000675939.1:c.463_478delinsAAGCGCACGCTGGAGG ENSP00000502256.1:p.Lys155=
ENST00000675989.1:n.838_853delinsAAGCGCACGCTGGAGG
ENST00000676208.1:c.463_478delinsAAGCGCACGCTGGAGG ENSP00000502468.1:p.Lys155=
ENST00000676283.1:n.838_853delinsAAGCGCACGCTGGAGG
ENST00000676385.2:c.463_478delinsAAGCGCACGCTGGAGG ENSP00000502091.1:p.Lys155=
ENST00000676434.1:c.463_478delinsAAGCGCACGCTGGAGG ENSP00000501648.1:p.Lys155=
ENST00000677389.1:c.463_478delinsAAGCGCACGCTGGAGG MANE Plus Clinical ENSP00000503633.1:p.Lys155=
ENST00000347559.6:c.463_478delinsAAGCGCACGCTGGAGG ENSP00000292304.3:p.Lys155=
ENST00000361308.8:c.463_478delinsAAGCGCACGCTGGAGG ENSP00000355292.5:p.Lys155=
ENST00000368297.5:c.220_235delinsAAGCGCACGCTGGAGG ENSP00000357280.1:p.Lys74=
ENST00000368299.7:c.463_478delinsAAGCGCACGCTGGAGG ENSP00000357282.3:p.Lys155=
ENST00000368300.8:c.463_478delinsAAGCGCACGCTGGAGG ENSP00000357283.4:p.Lys155=
ENST00000368301.6:c.463_478delinsAAGCGCACGCTGGAGG ENSP00000357284.2:p.Lys155=
ENST00000448611.6:c.127_142delinsAAGCGCACGCTGGAGG ENSP00000395597.2:p.Lys43=
ENST00000469565.6:n.497_512delinsAAGCGCACGCTGGAGG
ENST00000470199.2:n.405_420delinsAAGCGCACGCTGGAGG
ENST00000473598.6:c.166_181delinsAAGCGCACGCTGGAGG ENSP00000421821.1:p.Lys56=
ENST00000502357.5:n.361_376delinsAAGCGCACGCTGGAGG
ENST00000502751.5:n.435_450delinsAAGCGCACGCTGGAGG
ENST00000504687.5:c.214_229delinsAAGCGCACGCTGGAGG ENSP00000426535.1:p.Lys72=
ENST00000515459.5:c.*137_*152delinsAAGCGCACGCTGGAGG ENSP00000424518.1:n.*137_*152delinsAAGCGCACGCTGGAGG
NM_001257374.2:c.127_142delinsAAGCGCACGCTGGAGG NP_001244303.1:p.Lys43=
NM_001282624.1:c.220_235delinsAAGCGCACGCTGGAGG NP_001269553.1:p.Lys74=
NM_001282625.1:c.463_478delinsAAGCGCACGCTGGAGG NP_001269554.1:p.Lys155=
NM_001282626.1:c.463_478delinsAAGCGCACGCTGGAGG NP_001269555.1:p.Lys155=
NM_005572.3:c.463_478delinsAAGCGCACGCTGGAGG , LRG_254t1:c.463_478delinsAAGCGCACGCTGGAGG NP_005563.1:p.Lys155=
NM_170707.3:c.463_478delinsAAGCGCACGCTGGAGG NP_733821.1:p.Lys155=
NM_170708.3:c.463_478delinsAAGCGCACGCTGGAGG NP_733822.1:p.Lys155=
XM_011509533.1:c.127_142delinsAAGCGCACGCTGGAGG XP_011507835.1:p.Lys43=
XM_011509534.1:c.-202_-187delinsAAGCGCACGCTGGAGG XP_011507836.1:n.-202_-187delinsAAGCGCACGCTGGAGG
XR_921781.1:n.712_727delinsAAGCGCACGCTGGAGG
XM_011509534.2:c.-202_-187delinsAAGCGCACGCTGGAGG XP_011507836.1:n.-202_-187delinsAAGCGCACGCTGGAGG
XR_921781.2:n.710_725delinsAAGCGCACGCTGGAGG
NM_170707.4:c.463_478delinsAAGCGCACGCTGGAGG MANE Select NP_733821.1:p.Lys155=
NM_001257374.3:c.127_142delinsAAGCGCACGCTGGAGG NP_001244303.1:p.Lys43=
NM_001282626.2:c.463_478delinsAAGCGCACGCTGGAGG NP_001269555.1:p.Lys155=
NM_001282624.2:c.220_235delinsAAGCGCACGCTGGAGG NP_001269553.1:p.Lys74=
NM_001282625.2:c.463_478delinsAAGCGCACGCTGGAGG NP_001269554.1:p.Lys155=
NM_005572.4:c.463_478delinsAAGCGCACGCTGGAGG MANE Plus Clinical NP_005563.1:p.Lys155=
NM_170708.4:c.463_478delinsAAGCGCACGCTGGAGG NP_733822.1:p.Lys155=