Canonical Allele Identifier: CA1200473551
Gene: LMNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156138706C= , CM000663.2:g.156138706C= GRCh38
NC_000001.10:g.156108497C= , CM000663.1:g.156108497C= GRCh37
NC_000001.9:g.154375121C= NCBI36
NG_008692.2:g.61134C= , LRG_254:g.61134C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504687.7:c.1359C= ENSP00000426535.3:p.Asp453=
ENST00000682650.1:c.1827C= ENSP00000506904.1:p.Asp609=
ENST00000683032.1:c.1917C= ENSP00000506771.1:p.Asp639=
ENST00000683773.1:n.163+99C=
ENST00000684195.1:c.*1009C= ENSP00000508220.1:n.*1009C=
ENST00000361308.9:c.1917C= ENSP00000355292.6:p.Asp639=
ENST00000368300.9:c.1917C= MANE Select ENSP00000357283.4:p.Asp639=
ENST00000674518.1:c.*1267C= ENSP00000502261.1:n.*1267C=
ENST00000674600.1:c.*1716C= ENSP00000501666.1:n.*1716C=
ENST00000675455.1:c.*1717C= ENSP00000501795.1:n.*1717C=
ENST00000675667.1:c.1917C= ENSP00000501803.1:p.Asp639=
ENST00000675874.1:c.*1388C= ENSP00000501851.1:n.*1388C=
ENST00000675881.1:c.*928C= ENSP00000501670.1:n.*928C=
ENST00000675939.1:c.1917C= ENSP00000502256.1:p.Asp639=
ENST00000675989.1:n.3520C=
ENST00000676208.1:c.*1020C= ENSP00000502468.1:n.*1020C=
ENST00000676385.2:c.1827C= ENSP00000502091.1:p.Asp609=
ENST00000676434.1:c.*1672C= ENSP00000501648.1:n.*1672C=
ENST00000347559.6:c.1827C= ENSP00000292304.3:p.Asp609=
ENST00000368299.7:c.1818+99C= ENSP00000357282.3:n.1818+99C=
ENST00000368300.8:c.1917C= ENSP00000357283.4:p.Asp639=
ENST00000448611.6:c.1581C= ENSP00000395597.2:p.Asp527=
ENST00000473598.6:c.1620C= ENSP00000421821.1:p.Asp540=
ENST00000496738.5:n.2130C=
ENST00000506981.1:n.501C=
ENST00000508500.1:c.705C= ENSP00000424977.1:p.Asp235=
NM_001257374.2:c.1581C= NP_001244303.1:p.Asp527=
NM_001282626.1:c.1818+99C= NP_001269555.1:n.1818+99C=
NM_170707.3:c.1917C= NP_733821.1:p.Asp639=
NM_170708.3:c.1827C= NP_733822.1:p.Asp609=
XM_011509533.1:c.1581C= XP_011507835.1:p.Asp527=
XM_011509534.1:c.1293C= XP_011507836.1:p.Asp431=
XR_921781.1:n.2206C=
XM_011509534.2:c.1293C= XP_011507836.1:p.Asp431=
XR_921781.2:n.2204C=
NM_170707.4:c.1917C= MANE Select NP_733821.1:p.Asp639=
NM_001257374.3:c.1581C= NP_001244303.1:p.Asp527=
NM_001282626.2:c.1818+99C= NP_001269555.1:n.1818+99C=
NM_170708.4:c.1827C= NP_733822.1:p.Asp609=