Canonical Allele Identifier: CA1200467107

Gene: LMNA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156130290_156130292delinsCCT , CM000663.2:g.156130290_156130292delinsCCT	GRCh38
NC_000001.10:g.156100081_156100083delinsCCT , CM000663.1:g.156100081_156100083delinsCCT	GRCh37
NC_000001.9:g.154366705_154366707delinsCCT	NCBI36
NG_008692.2:g.52718_52720delinsCCT , LRG_254:g.52718_52720delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.-202-327_-202-325delinsCCT	ENSP00000426535.3:n.-202-327_-202-325delinsCCT
ENST00000682650.1:c.357-327_357-325delinsCCT	ENSP00000506904.1:n.357-327_357-325delinsCCT
ENST00000683032.1:c.357-327_357-325delinsCCT	ENSP00000506771.1:n.357-327_357-325delinsCCT
ENST00000684195.1:c.357-327_357-325delinsCCT	ENSP00000508220.1:n.357-327_357-325delinsCCT
ENST00000361308.9:c.357-327_357-325delinsCCT	ENSP00000355292.6:n.357-327_357-325delinsCCT
ENST00000368300.9:c.357-327_357-325delinsCCT MANE Select	ENSP00000357283.4:n.357-327_357-325delinsCCT
ENST00000496738.6:n.732-327_732-325delinsCCT
ENST00000504687.6:c.-308-327_-308-325delinsCCT	ENSP00000426535.2:n.-308-327_-308-325delinsCCT
ENST00000674518.1:c.357-327_357-325delinsCCT	ENSP00000502261.1:n.357-327_357-325delinsCCT
ENST00000674600.1:c.*156-327_*156-325delinsCCT	ENSP00000501666.1:n.*156-327_*156-325delinsCCT
ENST00000674720.1:c.357-327_357-325delinsCCT	ENSP00000502798.1:n.357-327_357-325delinsCCT
ENST00000675431.1:n.50-327_50-325delinsCCT
ENST00000675455.1:c.*157-327_*157-325delinsCCT	ENSP00000501795.1:n.*157-327_*157-325delinsCCT
ENST00000675667.1:c.357-327_357-325delinsCCT	ENSP00000501803.1:n.357-327_357-325delinsCCT
ENST00000675874.1:c.357-4113_357-4111delinsCCT	ENSP00000501851.1:n.357-4113_357-4111delinsCCT
ENST00000675881.1:c.357-327_357-325delinsCCT	ENSP00000501670.1:n.357-327_357-325delinsCCT
ENST00000675939.1:c.357-327_357-325delinsCCT	ENSP00000502256.1:n.357-327_357-325delinsCCT
ENST00000675989.1:n.732-327_732-325delinsCCT
ENST00000676208.1:c.357-327_357-325delinsCCT	ENSP00000502468.1:n.357-327_357-325delinsCCT
ENST00000676283.1:n.732-327_732-325delinsCCT
ENST00000676385.2:c.357-327_357-325delinsCCT	ENSP00000502091.1:n.357-327_357-325delinsCCT
ENST00000676434.1:c.357-327_357-325delinsCCT	ENSP00000501648.1:n.357-327_357-325delinsCCT
ENST00000677389.1:c.357-327_357-325delinsCCT MANE Plus Clinical	ENSP00000503633.1:n.357-327_357-325delinsCCT
ENST00000347559.6:c.357-327_357-325delinsCCT	ENSP00000292304.3:n.357-327_357-325delinsCCT
ENST00000361308.8:c.357-327_357-325delinsCCT	ENSP00000355292.5:n.357-327_357-325delinsCCT
ENST00000368297.5:c.114-327_114-325delinsCCT	ENSP00000357280.1:n.114-327_114-325delinsCCT
ENST00000368299.7:c.357-327_357-325delinsCCT	ENSP00000357282.3:n.357-327_357-325delinsCCT
ENST00000368300.8:c.357-327_357-325delinsCCT	ENSP00000357283.4:n.357-327_357-325delinsCCT
ENST00000368301.6:c.357-327_357-325delinsCCT	ENSP00000357284.2:n.357-327_357-325delinsCCT
ENST00000448611.6:c.21-327_21-325delinsCCT	ENSP00000395597.2:n.21-327_21-325delinsCCT
ENST00000469565.6:n.391-327_391-325delinsCCT
ENST00000470199.2:n.357-385_357-383delinsCCT
ENST00000473598.6:c.60-327_60-325delinsCCT	ENSP00000421821.1:n.60-327_60-325delinsCCT
ENST00000502357.5:n.255-327_255-325delinsCCT
ENST00000502751.5:n.329-327_329-325delinsCCT
ENST00000504687.5:c.108-327_108-325delinsCCT	ENSP00000426535.1:n.108-327_108-325delinsCCT
ENST00000515459.5:c.*31-327_*31-325delinsCCT	ENSP00000424518.1:n.*31-327_*31-325delinsCCT
NM_001257374.2:c.21-327_21-325delinsCCT	NP_001244303.1:n.21-327_21-325delinsCCT
NM_001282624.1:c.114-327_114-325delinsCCT	NP_001269553.1:n.114-327_114-325delinsCCT
NM_001282625.1:c.357-327_357-325delinsCCT	NP_001269554.1:n.357-327_357-325delinsCCT
NM_001282626.1:c.357-327_357-325delinsCCT	NP_001269555.1:n.357-327_357-325delinsCCT
NM_005572.3:c.357-327_357-325delinsCCT , LRG_254t1:c.357-327_357-325delinsCCT	NP_005563.1:n.357-327_357-325delinsCCT
NM_170707.3:c.357-327_357-325delinsCCT	NP_733821.1:n.357-327_357-325delinsCCT
NM_170708.3:c.357-327_357-325delinsCCT	NP_733822.1:n.357-327_357-325delinsCCT
XM_011509533.1:c.21-327_21-325delinsCCT	XP_011507835.1:n.21-327_21-325delinsCCT
XR_921781.1:n.606-327_606-325delinsCCT
XM_011509534.2:c.-308-327_-308-325delinsCCT	XP_011507836.1:n.-308-327_-308-325delinsCCT
XR_921781.2:n.604-327_604-325delinsCCT
NM_170707.4:c.357-327_357-325delinsCCT MANE Select	NP_733821.1:n.357-327_357-325delinsCCT
NM_001257374.3:c.21-327_21-325delinsCCT	NP_001244303.1:n.21-327_21-325delinsCCT
NM_001282626.2:c.357-327_357-325delinsCCT	NP_001269555.1:n.357-327_357-325delinsCCT
NM_001282624.2:c.114-327_114-325delinsCCT	NP_001269553.1:n.114-327_114-325delinsCCT
NM_001282625.2:c.357-327_357-325delinsCCT	NP_001269554.1:n.357-327_357-325delinsCCT
NM_005572.4:c.357-327_357-325delinsCCT MANE Plus Clinical	NP_005563.1:n.357-327_357-325delinsCCT
NM_170708.4:c.357-327_357-325delinsCCT	NP_733822.1:n.357-327_357-325delinsCCT