Canonical Allele Identifier: CA1140708212
Gene: LMNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156130679T= , CM000663.2:g.156130679T= GRCh38
NC_000001.10:g.156100470T= , CM000663.1:g.156100470T= GRCh37
NC_000001.9:g.154367094T= NCBI36
NG_008692.2:g.53107T= , LRG_254:g.53107T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504687.7:c.-140T= ENSP00000426535.3:n.-140T=
ENST00000682650.1:c.419T= ENSP00000506904.1:p.Leu140=
ENST00000683032.1:c.419T= ENSP00000506771.1:p.Leu140=
ENST00000684195.1:c.419T= ENSP00000508220.1:p.Leu140=
ENST00000361308.9:c.419T= ENSP00000355292.6:p.Leu140=
ENST00000368300.9:c.419T= MANE Select ENSP00000357283.4:p.Leu140=
ENST00000496738.6:n.794T=
ENST00000504687.6:c.-246T= ENSP00000426535.2:n.-246T=
ENST00000674518.1:c.419T= ENSP00000502261.1:p.Leu140=
ENST00000674600.1:c.*218T= ENSP00000501666.1:n.*218T=
ENST00000674720.1:c.419T= ENSP00000502798.1:p.Leu140=
ENST00000675431.1:n.112T=
ENST00000675455.1:c.*219T= ENSP00000501795.1:n.*219T=
ENST00000675667.1:c.419T= ENSP00000501803.1:p.Leu140=
ENST00000675874.1:c.357-3724T= ENSP00000501851.1:n.357-3724T=
ENST00000675881.1:c.419T= ENSP00000501670.1:p.Leu140=
ENST00000675939.1:c.419T= ENSP00000502256.1:p.Leu140=
ENST00000675989.1:n.794T=
ENST00000676208.1:c.419T= ENSP00000502468.1:p.Leu140=
ENST00000676283.1:n.794T=
ENST00000676385.2:c.419T= ENSP00000502091.1:p.Leu140=
ENST00000676434.1:c.419T= ENSP00000501648.1:p.Leu140=
ENST00000677389.1:c.419T= MANE Plus Clinical ENSP00000503633.1:p.Leu140=
ENST00000347559.6:c.419T= ENSP00000292304.3:p.Leu140=
ENST00000361308.8:c.419T= ENSP00000355292.5:p.Leu140=
ENST00000368297.5:c.176T= ENSP00000357280.1:p.Leu59=
ENST00000368299.7:c.419T= ENSP00000357282.3:p.Leu140=
ENST00000368300.8:c.419T= ENSP00000357283.4:p.Leu140=
ENST00000368301.6:c.419T= ENSP00000357284.2:p.Leu140=
ENST00000448611.6:c.83T= ENSP00000395597.2:p.Leu28=
ENST00000469565.6:n.453T=
ENST00000470199.2:n.361T=
ENST00000473598.6:c.122T= ENSP00000421821.1:p.Leu41=
ENST00000502357.5:n.317T=
ENST00000502751.5:n.391T=
ENST00000504687.5:c.170T= ENSP00000426535.1:p.Leu57=
ENST00000515459.5:c.*93T= ENSP00000424518.1:n.*93T=
NM_001257374.2:c.83T= NP_001244303.1:p.Leu28=
NM_001282624.1:c.176T= NP_001269553.1:p.Leu59=
NM_001282625.1:c.419T= NP_001269554.1:p.Leu140=
NM_001282626.1:c.419T= NP_001269555.1:p.Leu140=
NM_005572.3:c.419T= , LRG_254t1:c.419T= NP_005563.1:p.Leu140=
NM_170707.3:c.419T= NP_733821.1:p.Leu140=
NM_170708.3:c.419T= NP_733822.1:p.Leu140=
XM_011509533.1:c.83T= XP_011507835.1:p.Leu28=
XM_011509534.1:c.-246T= XP_011507836.1:n.-246T=
XR_921781.1:n.668T=
XM_011509534.2:c.-246T= XP_011507836.1:n.-246T=
XR_921781.2:n.666T=
NM_170707.4:c.419T= MANE Select NP_733821.1:p.Leu140=
NM_001257374.3:c.83T= NP_001244303.1:p.Leu28=
NM_001282626.2:c.419T= NP_001269555.1:p.Leu140=
NM_001282624.2:c.176T= NP_001269553.1:p.Leu59=
NM_001282625.2:c.419T= NP_001269554.1:p.Leu140=
NM_005572.4:c.419T= MANE Plus Clinical NP_005563.1:p.Leu140=
NM_170708.4:c.419T= NP_733822.1:p.Leu140=