Canonical Allele Identifier: CA421068820
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 751166
ClinVar RCV Id: RCV001455182
dbSNP Id: rs1278554399
MyVariant Identifiers: chr1:g.156106714C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156136923C>T , CM000663.2:g.156136923C>T GRCh38
NC_000001.10:g.156106714C>T , CM000663.1:g.156106714C>T GRCh37
NC_000001.9:g.154373338C>T NCBI36
NG_008692.2:g.59351C>T , LRG_254:g.59351C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000504687.7:c.825C>T ENSP00000426535.3:p.Asp275=
ENST00000459904.2:n.631C>T
ENST00000498722.3:n.615C>T
ENST00000682650.1:c.1383C>T ENSP00000506904.1:p.Asp461=
ENST00000683032.1:c.1383C>T ENSP00000506771.1:p.Asp461=
ENST00000684195.1:c.1383C>T ENSP00000508220.1:p.Asp461=
ENST00000361308.9:c.1383C>T ENSP00000355292.6:p.Asp461=
ENST00000368300.9:c.1383C>T MANE Select ENSP00000357283.4:p.Asp461=
ENST00000496738.6:n.1758C>T
ENST00000674518.1:c.*733C>T ENSP00000502261.1:n.*733C>T
ENST00000674600.1:c.*1182C>T ENSP00000501666.1:n.*1182C>T
ENST00000674720.1:c.1496C>T ENSP00000502798.1:p.Thr499Ile
ENST00000675431.1:n.1076C>T
ENST00000675455.1:c.*1183C>T ENSP00000501795.1:n.*1183C>T
ENST00000675667.1:c.1383C>T ENSP00000501803.1:p.Asp461=
ENST00000675874.1:c.*854C>T ENSP00000501851.1:n.*854C>T
ENST00000675881.1:c.*394C>T ENSP00000501670.1:n.*394C>T
ENST00000675939.1:c.1383C>T ENSP00000502256.1:p.Asp461=
ENST00000675989.1:n.2242C>T
ENST00000676208.1:c.*486C>T ENSP00000502468.1:n.*486C>T
ENST00000676283.1:n.1758C>T
ENST00000676385.2:c.1383C>T ENSP00000502091.1:p.Asp461=
ENST00000676434.1:c.*394C>T ENSP00000501648.1:n.*394C>T
ENST00000677389.1:c.1383C>T MANE Plus Clinical ENSP00000503633.1:p.Asp461=
ENST00000347559.6:c.1383C>T ENSP00000292304.3:p.Asp461=
ENST00000361308.8:c.1312-268C>T ENSP00000355292.5:n.1312-268C>T
ENST00000368297.5:c.1140C>T ENSP00000357280.1:p.Asp380=
ENST00000368298.2:n.1131C>T
ENST00000368299.7:c.1383C>T ENSP00000357282.3:p.Asp461=
ENST00000368300.8:c.1383C>T ENSP00000357283.4:p.Asp461=
ENST00000368301.6:c.1383C>T ENSP00000357284.2:p.Asp461=
ENST00000448611.6:c.1047C>T ENSP00000395597.2:p.Asp349=
ENST00000459904.1:n.631C>T
ENST00000473598.6:c.1086C>T ENSP00000421821.1:p.Asp362=
ENST00000496738.5:n.768C>T
ENST00000498722.2:n.615C>T
ENST00000508500.1:c.261C>T ENSP00000424977.1:p.Asp87=
NM_001257374.2:c.1047C>T NP_001244303.1:p.Asp349=
NM_001282624.1:c.1140C>T NP_001269553.1:p.Asp380=
NM_001282625.1:c.1383C>T NP_001269554.1:p.Asp461=
NM_001282626.1:c.1383C>T NP_001269555.1:p.Asp461=
NM_005572.3:c.1383C>T , LRG_254t1:c.1383C>T NP_005563.1:p.Asp461=
NM_170707.3:c.1383C>T NP_733821.1:p.Asp461=
NM_170708.3:c.1383C>T NP_733822.1:p.Asp461=
XM_011509533.1:c.1047C>T XP_011507835.1:p.Asp349=
XM_011509534.1:c.759C>T XP_011507836.1:p.Asp253=
XR_921781.1:n.1672C>T
XM_011509534.2:c.759C>T XP_011507836.1:p.Asp253=
XR_921781.2:n.1670C>T
NM_170707.4:c.1383C>T MANE Select NP_733821.1:p.Asp461=
NM_001257374.3:c.1047C>T NP_001244303.1:p.Asp349=
NM_001282626.2:c.1383C>T NP_001269555.1:p.Asp461=
NM_001282624.2:c.1140C>T NP_001269553.1:p.Asp380=
NM_001282625.2:c.1383C>T NP_001269554.1:p.Asp461=
NM_005572.4:c.1383C>T MANE Plus Clinical NP_005563.1:p.Asp461=
NM_170708.4:c.1383C>T NP_733822.1:p.Asp461=