Canonical Allele Identifier: CA1200472933
Gene: LMNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156137224A= , CM000663.2:g.156137224A= GRCh38
NC_000001.10:g.156107015A= , CM000663.1:g.156107015A= GRCh37
NC_000001.9:g.154373639A= NCBI36
NG_008692.2:g.59652A= , LRG_254:g.59652A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504687.7:c.1042A= ENSP00000426535.3:p.Thr348=
ENST00000459904.2:n.848A=
ENST00000498722.3:n.832A=
ENST00000682650.1:c.1600A= ENSP00000506904.1:p.Thr534=
ENST00000683032.1:c.1600A= ENSP00000506771.1:p.Thr534=
ENST00000684195.1:c.1579+21A= ENSP00000508220.1:n.1579+21A=
ENST00000361308.9:c.1600A= ENSP00000355292.6:p.Thr534=
ENST00000368300.9:c.1600A= MANE Select ENSP00000357283.4:p.Thr534=
ENST00000496738.6:n.2059A=
ENST00000674518.1:c.*950A= ENSP00000502261.1:n.*950A=
ENST00000674600.1:c.*1399A= ENSP00000501666.1:n.*1399A=
ENST00000674720.1:c.*162A= ENSP00000502798.1:n.*162A=
ENST00000675431.1:n.1293A=
ENST00000675455.1:c.*1400A= ENSP00000501795.1:n.*1400A=
ENST00000675667.1:c.1600A= ENSP00000501803.1:p.Thr534=
ENST00000675874.1:c.*1071A= ENSP00000501851.1:n.*1071A=
ENST00000675881.1:c.*611A= ENSP00000501670.1:n.*611A=
ENST00000675939.1:c.1600A= ENSP00000502256.1:p.Thr534=
ENST00000675989.1:n.2459A=
ENST00000676208.1:c.*703A= ENSP00000502468.1:n.*703A=
ENST00000676283.1:n.1975A=
ENST00000676385.2:c.1600A= ENSP00000502091.1:p.Thr534=
ENST00000676434.1:c.*611A= ENSP00000501648.1:n.*611A=
ENST00000677389.1:c.1600A= MANE Plus Clinical ENSP00000503633.1:p.Thr534=
ENST00000347559.6:c.1600A= ENSP00000292304.3:p.Thr534=
ENST00000361308.8:c.1345A= ENSP00000355292.5:p.Thr449=
ENST00000368297.5:c.1357A= ENSP00000357280.1:p.Thr453=
ENST00000368298.2:n.1432A=
ENST00000368299.7:c.1600A= ENSP00000357282.3:p.Thr534=
ENST00000368300.8:c.1600A= ENSP00000357283.4:p.Thr534=
ENST00000368301.6:c.1600A= ENSP00000357284.2:p.Thr534=
ENST00000448611.6:c.1264A= ENSP00000395597.2:p.Thr422=
ENST00000459904.1:n.848A=
ENST00000473598.6:c.1303A= ENSP00000421821.1:p.Thr435=
ENST00000496738.5:n.1069A=
ENST00000498722.2:n.832A=
ENST00000508500.1:c.478A= ENSP00000424977.1:p.Thr160=
NM_001257374.2:c.1264A= NP_001244303.1:p.Thr422=
NM_001282624.1:c.1357A= NP_001269553.1:p.Thr453=
NM_001282625.1:c.1600A= NP_001269554.1:p.Thr534=
NM_001282626.1:c.1600A= NP_001269555.1:p.Thr534=
NM_005572.3:c.1600A= , LRG_254t1:c.1600A= NP_005563.1:p.Thr534=
NM_170707.3:c.1600A= NP_733821.1:p.Thr534=
NM_170708.3:c.1600A= NP_733822.1:p.Thr534=
XM_011509533.1:c.1264A= XP_011507835.1:p.Thr422=
XM_011509534.1:c.976A= XP_011507836.1:p.Thr326=
XR_921781.1:n.1889A=
XM_011509534.2:c.976A= XP_011507836.1:p.Thr326=
XR_921781.2:n.1887A=
NM_170707.4:c.1600A= MANE Select NP_733821.1:p.Thr534=
NM_001257374.3:c.1264A= NP_001244303.1:p.Thr422=
NM_001282626.2:c.1600A= NP_001269555.1:p.Thr534=
NM_001282624.2:c.1357A= NP_001269553.1:p.Thr453=
NM_001282625.2:c.1600A= NP_001269554.1:p.Thr534=
NM_005572.4:c.1600A= MANE Plus Clinical NP_005563.1:p.Thr534=
NM_170708.4:c.1600A= NP_733822.1:p.Thr534=