Canonical Allele Identifier: CA1143538320
Gene: LMNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156134458G= , CM000663.2:g.156134458G= GRCh38
NC_000001.10:g.156104249G= , CM000663.1:g.156104249G= GRCh37
NC_000001.9:g.154370873G= NCBI36
NG_008692.2:g.56886G= , LRG_254:g.56886G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504687.7:c.11G= ENSP00000426535.3:p.Arg4=
ENST00000682650.1:c.569G= ENSP00000506904.1:p.Arg190=
ENST00000683032.1:c.569G= ENSP00000506771.1:p.Arg190=
ENST00000684195.1:c.569G= ENSP00000508220.1:p.Arg190=
ENST00000361308.9:c.569G= ENSP00000355292.6:p.Arg190=
ENST00000368300.9:c.569G= MANE Select ENSP00000357283.4:p.Arg190=
ENST00000496738.6:n.944G=
ENST00000504687.6:c.-96G= ENSP00000426535.2:n.-96G=
ENST00000674518.1:c.569G= ENSP00000502261.1:p.Arg190=
ENST00000674600.1:c.*368G= ENSP00000501666.1:n.*368G=
ENST00000674720.1:c.569G= ENSP00000502798.1:p.Arg190=
ENST00000675431.1:n.262G=
ENST00000675455.1:c.*369G= ENSP00000501795.1:n.*369G=
ENST00000675667.1:c.569G= ENSP00000501803.1:p.Arg190=
ENST00000675874.1:c.*40G= ENSP00000501851.1:n.*40G=
ENST00000675881.1:c.569G= ENSP00000501670.1:p.Arg190=
ENST00000675939.1:c.569G= ENSP00000502256.1:p.Arg190=
ENST00000675989.1:n.944G=
ENST00000676208.1:c.569G= ENSP00000502468.1:p.Arg190=
ENST00000676283.1:n.944G=
ENST00000676385.2:c.569G= ENSP00000502091.1:p.Arg190=
ENST00000676434.1:c.569G= ENSP00000501648.1:p.Arg190=
ENST00000677389.1:c.569G= MANE Plus Clinical ENSP00000503633.1:p.Arg190=
ENST00000347559.6:c.569G= ENSP00000292304.3:p.Arg190=
ENST00000361308.8:c.569G= ENSP00000355292.5:p.Arg190=
ENST00000368297.5:c.326G= ENSP00000357280.1:p.Arg109=
ENST00000368299.7:c.569G= ENSP00000357282.3:p.Arg190=
ENST00000368300.8:c.569G= ENSP00000357283.4:p.Arg190=
ENST00000368301.6:c.569G= ENSP00000357284.2:p.Arg190=
ENST00000448611.6:c.233G= ENSP00000395597.2:p.Arg78=
ENST00000470199.2:n.511G=
ENST00000473598.6:c.272G= ENSP00000421821.1:p.Arg91=
ENST00000502357.5:n.467G=
ENST00000502751.5:n.541G=
ENST00000504687.5:c.320G= ENSP00000426535.1:p.Arg107=
ENST00000515459.5:c.*243G= ENSP00000424518.1:n.*243G=
NM_001257374.2:c.233G= NP_001244303.1:p.Arg78=
NM_001282624.1:c.326G= NP_001269553.1:p.Arg109=
NM_001282625.1:c.569G= NP_001269554.1:p.Arg190=
NM_001282626.1:c.569G= NP_001269555.1:p.Arg190=
NM_005572.3:c.569G= , LRG_254t1:c.569G= NP_005563.1:p.Arg190=
NM_170707.3:c.569G= NP_733821.1:p.Arg190=
NM_170708.3:c.569G= NP_733822.1:p.Arg190=
XM_011509533.1:c.233G= XP_011507835.1:p.Arg78=
XM_011509534.1:c.-96G= XP_011507836.1:n.-96G=
XR_921781.1:n.818G=
XM_011509534.2:c.-96G= XP_011507836.1:n.-96G=
XR_921781.2:n.816G=
NM_170707.4:c.569G= MANE Select NP_733821.1:p.Arg190=
NM_001257374.3:c.233G= NP_001244303.1:p.Arg78=
NM_001282626.2:c.569G= NP_001269555.1:p.Arg190=
NM_001282624.2:c.326G= NP_001269553.1:p.Arg109=
NM_001282625.2:c.569G= NP_001269554.1:p.Arg190=
NM_005572.4:c.569G= MANE Plus Clinical NP_005563.1:p.Arg190=
NM_170708.4:c.569G= NP_733822.1:p.Arg190=