Canonical Allele Identifier: CA1200471932
Gene: LMNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156134879G= , CM000663.2:g.156134879G= GRCh38
NC_000001.10:g.156104670G= , CM000663.1:g.156104670G= GRCh37
NC_000001.9:g.154371294G= NCBI36
NG_008692.2:g.57307G= , LRG_254:g.57307G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504687.7:c.156G= ENSP00000426535.3:p.Glu52=
ENST00000682650.1:c.714G= ENSP00000506904.1:p.Glu238=
ENST00000683032.1:c.714G= ENSP00000506771.1:p.Glu238=
ENST00000684195.1:c.714G= ENSP00000508220.1:p.Glu238=
ENST00000361308.9:c.714G= ENSP00000355292.6:p.Glu238=
ENST00000368300.9:c.714G= MANE Select ENSP00000357283.4:p.Glu238=
ENST00000496738.6:n.1089G=
ENST00000504687.6:c.50G= ENSP00000426535.2:p.Arg17=
ENST00000674518.1:c.*64G= ENSP00000502261.1:n.*64G=
ENST00000674600.1:c.*513G= ENSP00000501666.1:n.*513G=
ENST00000674720.1:c.714G= ENSP00000502798.1:p.Glu238=
ENST00000675431.1:n.407G=
ENST00000675455.1:c.*514G= ENSP00000501795.1:n.*514G=
ENST00000675667.1:c.714G= ENSP00000501803.1:p.Glu238=
ENST00000675874.1:c.*185G= ENSP00000501851.1:n.*185G=
ENST00000675881.1:c.714G= ENSP00000501670.1:p.Glu238=
ENST00000675939.1:c.714G= ENSP00000502256.1:p.Glu238=
ENST00000675989.1:n.1089G=
ENST00000676208.1:c.714G= ENSP00000502468.1:p.Glu238=
ENST00000676283.1:n.1089G=
ENST00000676385.2:c.714G= ENSP00000502091.1:p.Glu238=
ENST00000676434.1:c.714G= ENSP00000501648.1:p.Glu238=
ENST00000677389.1:c.714G= MANE Plus Clinical ENSP00000503633.1:p.Glu238=
ENST00000347559.6:c.714G= ENSP00000292304.3:p.Glu238=
ENST00000361308.8:c.714G= ENSP00000355292.5:p.Glu238=
ENST00000368297.5:c.471G= ENSP00000357280.1:p.Glu157=
ENST00000368299.7:c.714G= ENSP00000357282.3:p.Glu238=
ENST00000368300.8:c.714G= ENSP00000357283.4:p.Glu238=
ENST00000368301.6:c.714G= ENSP00000357284.2:p.Glu238=
ENST00000448611.6:c.378G= ENSP00000395597.2:p.Glu126=
ENST00000473598.6:c.417G= ENSP00000421821.1:p.Glu139=
ENST00000496738.5:n.59G=
ENST00000504687.5:c.465G= ENSP00000426535.1:p.Glu155=
ENST00000515459.5:c.*388G= ENSP00000424518.1:n.*388G=
ENST00000515824.1:n.75G=
NM_001257374.2:c.378G= NP_001244303.1:p.Glu126=
NM_001282624.1:c.471G= NP_001269553.1:p.Glu157=
NM_001282625.1:c.714G= NP_001269554.1:p.Glu238=
NM_001282626.1:c.714G= NP_001269555.1:p.Glu238=
NM_005572.3:c.714G= , LRG_254t1:c.714G= NP_005563.1:p.Glu238=
NM_170707.3:c.714G= NP_733821.1:p.Glu238=
NM_170708.3:c.714G= NP_733822.1:p.Glu238=
XM_011509533.1:c.378G= XP_011507835.1:p.Glu126=
XM_011509534.1:c.50G= XP_011507836.1:p.Arg17=
XR_921781.1:n.963G=
XM_011509534.2:c.50G= XP_011507836.1:p.Arg17=
XR_921781.2:n.961G=
NM_170707.4:c.714G= MANE Select NP_733821.1:p.Glu238=
NM_001257374.3:c.378G= NP_001244303.1:p.Glu126=
NM_001282626.2:c.714G= NP_001269555.1:p.Glu238=
NM_001282624.2:c.471G= NP_001269553.1:p.Glu157=
NM_001282625.2:c.714G= NP_001269554.1:p.Glu238=
NM_005572.4:c.714G= MANE Plus Clinical NP_005563.1:p.Glu238=
NM_170708.4:c.714G= NP_733822.1:p.Glu238=