Canonical Allele Identifier: CA342817719
Community Standard Title: NM_170707.4(LMNA):c.878A>T (p.Gln293Leu)
Gene: LMNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156135254A>T , CM000663.2:g.156135254A>T GRCh38
NC_000001.10:g.156105045A>T , CM000663.1:g.156105045A>T GRCh37
NC_000001.9:g.154371669A>T NCBI36
NG_008692.2:g.57682A>T , LRG_254:g.57682A>T

Transcript Alleles

HGVS Amino-acid Change
NM_170707.4:c.878A>T MANE Select NP_733821.1:p.Gln293Leu
ENST00000368300.9:c.878A>T MANE Select ENSP00000357283.4:p.Gln293Leu
NM_005572.4:c.878A>T MANE Plus Clinical NP_005563.1:p.Gln293Leu
ENST00000677389.1:c.878A>T MANE Plus Clinical ENSP00000503633.1:p.Gln293Leu
NM_001257374.2:c.542A>T NP_001244303.1:p.Gln181Leu
NM_001257374.3:c.542A>T NP_001244303.1:p.Gln181Leu
NM_001282624.1:c.635A>T NP_001269553.1:p.Gln212Leu
NM_001282624.2:c.635A>T NP_001269553.1:p.Gln212Leu
NM_001282625.1:c.878A>T NP_001269554.1:p.Gln293Leu
NM_001282625.2:c.878A>T NP_001269554.1:p.Gln293Leu
NM_001282626.1:c.878A>T NP_001269555.1:p.Gln293Leu
NM_001282626.2:c.878A>T NP_001269555.1:p.Gln293Leu
NM_005572.3:c.878A>T , LRG_254t1:c.878A>T NP_005563.1:p.Gln293Leu
NM_170707.3:c.878A>T NP_733821.1:p.Gln293Leu
NM_170708.3:c.878A>T NP_733822.1:p.Gln293Leu
NM_170708.4:c.878A>T NP_733822.1:p.Gln293Leu
ENST00000347559.6:c.878A>T ENSP00000292304.3:p.Gln293Leu
ENST00000361308.8:c.878A>T ENSP00000355292.5:p.Gln293Leu
ENST00000361308.9:c.878A>T ENSP00000355292.6:p.Gln293Leu
ENST00000368297.5:c.635A>T ENSP00000357280.1:p.Gln212Leu
ENST00000368298.2:n.142A>T
ENST00000368299.7:c.878A>T ENSP00000357282.3:p.Gln293Leu
ENST00000368300.8:c.878A>T ENSP00000357283.4:p.Gln293Leu
ENST00000368301.6:c.878A>T ENSP00000357284.2:p.Gln293Leu
ENST00000448611.6:c.542A>T ENSP00000395597.2:p.Gln181Leu
ENST00000473598.6:c.581A>T ENSP00000421821.1:p.Gln194Leu
ENST00000496738.5:n.223A>T
ENST00000496738.6:n.1253A>T
ENST00000504687.7:c.320A>T ENSP00000426535.3:p.Gln107Leu
ENST00000515824.1:n.239A>T
ENST00000674518.1:c.*228A>T ENSP00000502261.1:n.*228A>T
ENST00000674600.1:c.*677A>T ENSP00000501666.1:n.*677A>T
ENST00000674720.1:c.878A>T ENSP00000502798.1:p.Gln293Leu
ENST00000675431.1:n.571A>T
ENST00000675455.1:c.*678A>T ENSP00000501795.1:n.*678A>T
ENST00000675667.1:c.878A>T ENSP00000501803.1:p.Gln293Leu
ENST00000675874.1:c.*349A>T ENSP00000501851.1:n.*349A>T
ENST00000675881.1:c.878A>T ENSP00000501670.1:p.Gln293Leu
ENST00000675939.1:c.878A>T ENSP00000502256.1:p.Gln293Leu
ENST00000675989.1:n.1253A>T
ENST00000676208.1:c.878A>T ENSP00000502468.1:p.Gln293Leu
ENST00000676283.1:n.1253A>T
ENST00000676385.2:c.878A>T ENSP00000502091.1:p.Gln293Leu
ENST00000676434.1:c.878A>T ENSP00000501648.1:p.Gln293Leu
ENST00000682650.1:c.878A>T ENSP00000506904.1:p.Gln293Leu
ENST00000683032.1:c.878A>T ENSP00000506771.1:p.Gln293Leu
ENST00000684195.1:c.878A>T ENSP00000508220.1:p.Gln293Leu
XM_011509533.1:c.542A>T XP_011507835.1:p.Gln181Leu
XM_011509534.1:c.214A>T XP_011507836.1:p.Ser72Cys
XM_011509534.2:c.214A>T XP_011507836.1:p.Ser72Cys
XR_921781.1:n.1127A>T
XR_921781.2:n.1125A>T