Canonical Allele Identifier: CA1200472877

Gene: LMNA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156137116_156137117delinsTG , CM000663.2:g.156137116_156137117delinsTG	GRCh38
NC_000001.10:g.156106907_156106908delinsTG , CM000663.1:g.156106907_156106908delinsTG	GRCh37
NC_000001.9:g.154373531_154373532delinsTG	NCBI36
NG_008692.2:g.59544_59545delinsTG , LRG_254:g.59544_59545delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.934_935delinsTG	ENSP00000426535.3:p.Trp312=
ENST00000459904.2:n.740_741delinsTG
ENST00000498722.3:n.724_725delinsTG
ENST00000682650.1:c.1492_1493delinsTG	ENSP00000506904.1:p.Trp498=
ENST00000683032.1:c.1492_1493delinsTG	ENSP00000506771.1:p.Trp498=
ENST00000684195.1:c.1492_1493delinsTG	ENSP00000508220.1:p.Trp498=
ENST00000361308.9:c.1492_1493delinsTG	ENSP00000355292.6:p.Trp498=
ENST00000368300.9:c.1492_1493delinsTG MANE Select	ENSP00000357283.4:p.Trp498=
ENST00000496738.6:n.1951_1952delinsTG
ENST00000674518.1:c.*842_*843delinsTG	ENSP00000502261.1:n.*842_*843delinsTG
ENST00000674600.1:c.*1291_*1292delinsTG	ENSP00000501666.1:n.*1291_*1292delinsTG
ENST00000674720.1:c.*54_*55delinsTG	ENSP00000502798.1:n.*54_*55delinsTG
ENST00000675431.1:n.1185_1186delinsTG
ENST00000675455.1:c.*1292_*1293delinsTG	ENSP00000501795.1:n.*1292_*1293delinsTG
ENST00000675667.1:c.1492_1493delinsTG	ENSP00000501803.1:p.Trp498=
ENST00000675874.1:c.*963_*964delinsTG	ENSP00000501851.1:n.*963_*964delinsTG
ENST00000675881.1:c.*503_*504delinsTG	ENSP00000501670.1:n.*503_*504delinsTG
ENST00000675939.1:c.1492_1493delinsTG	ENSP00000502256.1:p.Trp498=
ENST00000675989.1:n.2351_2352delinsTG
ENST00000676208.1:c.*595_*596delinsTG	ENSP00000502468.1:n.*595_*596delinsTG
ENST00000676283.1:n.1867_1868delinsTG
ENST00000676385.2:c.1492_1493delinsTG	ENSP00000502091.1:p.Trp498=
ENST00000676434.1:c.*503_*504delinsTG	ENSP00000501648.1:n.*503_*504delinsTG
ENST00000677389.1:c.1492_1493delinsTG MANE Plus Clinical	ENSP00000503633.1:p.Trp498=
ENST00000347559.6:c.1492_1493delinsTG	ENSP00000292304.3:p.Trp498=
ENST00000361308.8:c.1312-75_1312-74delinsTG	ENSP00000355292.5:n.1312-75_1312-74delinsTG
ENST00000368297.5:c.1249_1250delinsTG	ENSP00000357280.1:p.Trp417=
ENST00000368298.2:n.1324_1325delinsTG
ENST00000368299.7:c.1492_1493delinsTG	ENSP00000357282.3:p.Trp498=
ENST00000368300.8:c.1492_1493delinsTG	ENSP00000357283.4:p.Trp498=
ENST00000368301.6:c.1492_1493delinsTG	ENSP00000357284.2:p.Trp498=
ENST00000448611.6:c.1156_1157delinsTG	ENSP00000395597.2:p.Trp386=
ENST00000459904.1:n.740_741delinsTG
ENST00000473598.6:c.1195_1196delinsTG	ENSP00000421821.1:p.Trp399=
ENST00000496738.5:n.961_962delinsTG
ENST00000498722.2:n.724_725delinsTG
ENST00000508500.1:c.370_371delinsTG	ENSP00000424977.1:p.Trp124=
NM_001257374.2:c.1156_1157delinsTG	NP_001244303.1:p.Trp386=
NM_001282624.1:c.1249_1250delinsTG	NP_001269553.1:p.Trp417=
NM_001282625.1:c.1492_1493delinsTG	NP_001269554.1:p.Trp498=
NM_001282626.1:c.1492_1493delinsTG	NP_001269555.1:p.Trp498=
NM_005572.3:c.1492_1493delinsTG , LRG_254t1:c.1492_1493delinsTG	NP_005563.1:p.Trp498=
NM_170707.3:c.1492_1493delinsTG	NP_733821.1:p.Trp498=
NM_170708.3:c.1492_1493delinsTG	NP_733822.1:p.Trp498=
XM_011509533.1:c.1156_1157delinsTG	XP_011507835.1:p.Trp386=
XM_011509534.1:c.868_869delinsTG	XP_011507836.1:p.Trp290=
XR_921781.1:n.1781_1782delinsTG
XM_011509534.2:c.868_869delinsTG	XP_011507836.1:p.Trp290=
XR_921781.2:n.1779_1780delinsTG
NM_170707.4:c.1492_1493delinsTG MANE Select	NP_733821.1:p.Trp498=
NM_001257374.3:c.1156_1157delinsTG	NP_001244303.1:p.Trp386=
NM_001282626.2:c.1492_1493delinsTG	NP_001269555.1:p.Trp498=
NM_001282624.2:c.1249_1250delinsTG	NP_001269553.1:p.Trp417=
NM_001282625.2:c.1492_1493delinsTG	NP_001269554.1:p.Trp498=
NM_005572.4:c.1492_1493delinsTG MANE Plus Clinical	NP_005563.1:p.Trp498=
NM_170708.4:c.1492_1493delinsTG	NP_733822.1:p.Trp498=