Canonical Allele Identifier: CA018917
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48097
dbSNP Id: rs56851164

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156135940T>A , CM000663.2:g.156135940T>A GRCh38
NC_000001.10:g.156105731T>A , CM000663.1:g.156105731T>A GRCh37
NC_000001.9:g.154372355T>A NCBI36
NG_008692.2:g.58368T>A , LRG_254:g.58368T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000504687.7:c.418T>A ENSP00000426535.3:p.Ser140Thr
ENST00000498722.3:n.208T>A
ENST00000682650.1:c.976T>A ENSP00000506904.1:p.Ser326Thr
ENST00000683032.1:c.976T>A ENSP00000506771.1:p.Ser326Thr
ENST00000684195.1:c.976T>A ENSP00000508220.1:p.Ser326Thr
ENST00000361308.9:c.976T>A ENSP00000355292.6:p.Ser326Thr
ENST00000368300.9:c.976T>A MANE Select ENSP00000357283.4:p.Ser326Thr
ENST00000496738.6:n.1351T>A
ENST00000674518.1:c.*326T>A ENSP00000502261.1:n.*326T>A
ENST00000674600.1:c.*775T>A ENSP00000501666.1:n.*775T>A
ENST00000674720.1:c.976T>A ENSP00000502798.1:p.Ser326Thr
ENST00000675431.1:n.669T>A
ENST00000675455.1:c.*776T>A ENSP00000501795.1:n.*776T>A
ENST00000675667.1:c.976T>A ENSP00000501803.1:p.Ser326Thr
ENST00000675874.1:c.*447T>A ENSP00000501851.1:n.*447T>A
ENST00000675881.1:c.1016T>A ENSP00000501670.1:p.Leu339His
ENST00000675939.1:c.976T>A ENSP00000502256.1:p.Ser326Thr
ENST00000675989.1:n.1351T>A
ENST00000676208.1:c.1016T>A ENSP00000502468.1:p.Leu339His
ENST00000676283.1:n.1351T>A
ENST00000676385.2:c.976T>A ENSP00000502091.1:p.Ser326Thr
ENST00000676434.1:c.1016T>A ENSP00000501648.1:p.Leu339His
ENST00000677389.1:c.976T>A MANE Plus Clinical ENSP00000503633.1:p.Ser326Thr
ENST00000347559.6:c.976T>A ENSP00000292304.3:p.Ser326Thr
ENST00000361308.8:c.976T>A ENSP00000355292.5:p.Ser326Thr
ENST00000368297.5:c.733T>A ENSP00000357280.1:p.Ser245Thr
ENST00000368298.2:n.240T>A
ENST00000368299.7:c.976T>A ENSP00000357282.3:p.Ser326Thr
ENST00000368300.8:c.976T>A ENSP00000357283.4:p.Ser326Thr
ENST00000368301.6:c.976T>A ENSP00000357284.2:p.Ser326Thr
ENST00000448611.6:c.640T>A ENSP00000395597.2:p.Ser214Thr
ENST00000473598.6:c.679T>A ENSP00000421821.1:p.Ser227Thr
ENST00000496738.5:n.361T>A
ENST00000498722.2:n.208T>A
NM_001257374.2:c.640T>A NP_001244303.1:p.Ser214Thr
NM_001282624.1:c.733T>A NP_001269553.1:p.Ser245Thr
NM_001282625.1:c.976T>A NP_001269554.1:p.Ser326Thr
NM_001282626.1:c.976T>A NP_001269555.1:p.Ser326Thr
NM_005572.3:c.976T>A , LRG_254t1:c.976T>A NP_005563.1:p.Ser326Thr
NM_170707.3:c.976T>A NP_733821.1:p.Ser326Thr
NM_170708.3:c.976T>A NP_733822.1:p.Ser326Thr
XM_011509533.1:c.640T>A XP_011507835.1:p.Ser214Thr
XM_011509534.1:c.352T>A XP_011507836.1:p.Ser118Thr
XR_921781.1:n.1265T>A
XM_011509534.2:c.352T>A XP_011507836.1:p.Ser118Thr
XR_921781.2:n.1263T>A
NM_170707.4:c.976T>A MANE Select NP_733821.1:p.Ser326Thr
NM_001257374.3:c.640T>A NP_001244303.1:p.Ser214Thr
NM_001282626.2:c.976T>A NP_001269555.1:p.Ser326Thr
NM_001282624.2:c.733T>A NP_001269553.1:p.Ser245Thr
NM_001282625.2:c.976T>A NP_001269554.1:p.Ser326Thr
NM_005572.4:c.976T>A MANE Plus Clinical NP_005563.1:p.Ser326Thr
NM_170708.4:c.976T>A NP_733822.1:p.Ser326Thr