Canonical Allele Identifier: CA2574066306
Gene: LMNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156135034dup , CM000663.2:g.156135034dup GRCh38
NC_000001.10:g.156104825dup , CM000663.1:g.156104825dup GRCh37
NC_000001.9:g.154371449dup NCBI36
NG_008692.2:g.57462dup , LRG_254:g.57462dup

Transcript Alleles

HGVS Amino-acid change
ENST00000504687.7:c.252+59dup ENSP00000426535.3:n.252+59dup
ENST00000682650.1:c.810+59dup ENSP00000506904.1:n.810+59dup
ENST00000683032.1:c.810+59dup ENSP00000506771.1:n.810+59dup
ENST00000684195.1:c.810+59dup ENSP00000508220.1:n.810+59dup
ENST00000361308.9:c.810+59dup ENSP00000355292.6:n.810+59dup
ENST00000368300.9:c.810+59dup MANE Select ENSP00000357283.4:n.810+59dup
ENST00000496738.6:n.1185+59dup
ENST00000674518.1:c.*160+59dup ENSP00000502261.1:n.*160+59dup
ENST00000674600.1:c.*609+59dup ENSP00000501666.1:n.*609+59dup
ENST00000674720.1:c.810+59dup ENSP00000502798.1:n.810+59dup
ENST00000675431.1:n.503+59dup
ENST00000675455.1:c.*610+59dup ENSP00000501795.1:n.*610+59dup
ENST00000675667.1:c.810+59dup ENSP00000501803.1:n.810+59dup
ENST00000675874.1:c.*281+59dup ENSP00000501851.1:n.*281+59dup
ENST00000675881.1:c.810+59dup ENSP00000501670.1:n.810+59dup
ENST00000675939.1:c.810+59dup ENSP00000502256.1:n.810+59dup
ENST00000675989.1:n.1185+59dup
ENST00000676208.1:c.810+59dup ENSP00000502468.1:n.810+59dup
ENST00000676283.1:n.1185+59dup
ENST00000676385.2:c.810+59dup ENSP00000502091.1:n.810+59dup
ENST00000676434.1:c.810+59dup ENSP00000501648.1:n.810+59dup
ENST00000677389.1:c.810+59dup MANE Plus Clinical ENSP00000503633.1:n.810+59dup
ENST00000347559.6:c.810+59dup ENSP00000292304.3:n.810+59dup
ENST00000361308.8:c.810+59dup ENSP00000355292.5:n.810+59dup
ENST00000368297.5:c.567+59dup ENSP00000357280.1:n.567+59dup
ENST00000368299.7:c.810+59dup ENSP00000357282.3:n.810+59dup
ENST00000368300.8:c.810+59dup ENSP00000357283.4:n.810+59dup
ENST00000368301.6:c.810+59dup ENSP00000357284.2:n.810+59dup
ENST00000448611.6:c.474+59dup ENSP00000395597.2:n.474+59dup
ENST00000473598.6:c.513+59dup ENSP00000421821.1:n.513+59dup
ENST00000496738.5:n.155+59dup
ENST00000515459.5:c.*484+59dup ENSP00000424518.1:n.*484+59dup
ENST00000515824.1:n.171+59dup
NM_001257374.2:c.474+59dup NP_001244303.1:n.474+59dup
NM_001282624.1:c.567+59dup NP_001269553.1:n.567+59dup
NM_001282625.1:c.810+59dup NP_001269554.1:n.810+59dup
NM_001282626.1:c.810+59dup NP_001269555.1:n.810+59dup
NM_005572.3:c.810+59dup , LRG_254t1:c.810+59dup NP_005563.1:n.810+59dup
NM_170707.3:c.810+59dup NP_733821.1:n.810+59dup
NM_170708.3:c.810+59dup NP_733822.1:n.810+59dup
XM_011509533.1:c.474+59dup XP_011507835.1:n.474+59dup
XM_011509534.1:c.146+59dup XP_011507836.1:n.146+59dup
XR_921781.1:n.1059+59dup
XM_011509534.2:c.146+59dup XP_011507836.1:n.146+59dup
XR_921781.2:n.1057+59dup
NM_170707.4:c.810+59dup MANE Select NP_733821.1:n.810+59dup
NM_001257374.3:c.474+59dup NP_001244303.1:n.474+59dup
NM_001282626.2:c.810+59dup NP_001269555.1:n.810+59dup
NM_001282624.2:c.567+59dup NP_001269553.1:n.567+59dup
NM_001282625.2:c.810+59dup NP_001269554.1:n.810+59dup
NM_005572.4:c.810+59dup MANE Plus Clinical NP_005563.1:n.810+59dup
NM_170708.4:c.810+59dup NP_733822.1:n.810+59dup