Canonical Allele Identifier: CA2648348916

Gene: LMNA

Linked Data

• gnomAD v4: 1-156135482-CCTGTGTGCTGTTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156135487_156135499del , CM000663.2:g.156135487_156135499del	GRCh38
NC_000001.10:g.156105278_156105290del , CM000663.1:g.156105278_156105290del	GRCh37
NC_000001.9:g.154371902_154371914del	NCBI36
NG_008692.2:g.57915_57927del , LRG_254:g.57915_57927del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.378+175_378+187del	ENSP00000426535.3:n.378+175_378+187del
ENST00000682650.1:c.936+175_936+187del	ENSP00000506904.1:n.936+175_936+187del
ENST00000683032.1:c.936+175_936+187del	ENSP00000506771.1:n.936+175_936+187del
ENST00000684195.1:c.936+175_936+187del	ENSP00000508220.1:n.936+175_936+187del
ENST00000361308.9:c.936+175_936+187del	ENSP00000355292.6:n.936+175_936+187del
ENST00000368300.9:c.936+175_936+187del MANE Select	ENSP00000357283.4:n.936+175_936+187del
ENST00000496738.6:n.1311+175_1311+187del
ENST00000674518.1:c.*286+175_*286+187del	ENSP00000502261.1:n.*286+175_*286+187del
ENST00000674600.1:c.*735+175_*735+187del	ENSP00000501666.1:n.*735+175_*735+187del
ENST00000674720.1:c.936+175_936+187del	ENSP00000502798.1:n.936+175_936+187del
ENST00000675431.1:n.629+175_629+187del
ENST00000675455.1:c.*736+175_*736+187del	ENSP00000501795.1:n.*736+175_*736+187del
ENST00000675667.1:c.936+175_936+187del	ENSP00000501803.1:n.936+175_936+187del
ENST00000675874.1:c.*407+175_*407+187del	ENSP00000501851.1:n.*407+175_*407+187del
ENST00000675881.1:c.936+175_936+187del	ENSP00000501670.1:n.936+175_936+187del
ENST00000675939.1:c.936+175_936+187del	ENSP00000502256.1:n.936+175_936+187del
ENST00000675989.1:n.1311+175_1311+187del
ENST00000676208.1:c.936+175_936+187del	ENSP00000502468.1:n.936+175_936+187del
ENST00000676283.1:n.1311+175_1311+187del
ENST00000676385.2:c.936+175_936+187del	ENSP00000502091.1:n.936+175_936+187del
ENST00000676434.1:c.936+175_936+187del	ENSP00000501648.1:n.936+175_936+187del
ENST00000677389.1:c.936+175_936+187del MANE Plus Clinical	ENSP00000503633.1:n.936+175_936+187del
ENST00000347559.6:c.936+175_936+187del	ENSP00000292304.3:n.936+175_936+187del
ENST00000361308.8:c.936+175_936+187del	ENSP00000355292.5:n.936+175_936+187del
ENST00000368297.5:c.693+175_693+187del	ENSP00000357280.1:n.693+175_693+187del
ENST00000368298.2:n.200+175_200+187del
ENST00000368299.7:c.936+175_936+187del	ENSP00000357282.3:n.936+175_936+187del
ENST00000368300.8:c.936+175_936+187del	ENSP00000357283.4:n.936+175_936+187del
ENST00000368301.6:c.936+175_936+187del	ENSP00000357284.2:n.936+175_936+187del
ENST00000448611.6:c.600+175_600+187del	ENSP00000395597.2:n.600+175_600+187del
ENST00000473598.6:c.639+175_639+187del	ENSP00000421821.1:n.639+175_639+187del
ENST00000496738.5:n.281+175_281+187del
NM_001257374.2:c.600+175_600+187del	NP_001244303.1:n.600+175_600+187del
NM_001282624.1:c.693+175_693+187del	NP_001269553.1:n.693+175_693+187del
NM_001282625.1:c.936+175_936+187del	NP_001269554.1:n.936+175_936+187del
NM_001282626.1:c.936+175_936+187del	NP_001269555.1:n.936+175_936+187del
NM_005572.3:c.936+175_936+187del , LRG_254t1:c.936+175_936+187del	NP_005563.1:n.936+175_936+187del
NM_170707.3:c.936+175_936+187del	NP_733821.1:n.936+175_936+187del
NM_170708.3:c.936+175_936+187del	NP_733822.1:n.936+175_936+187del
XM_011509533.1:c.600+175_600+187del	XP_011507835.1:n.600+175_600+187del
XM_011509534.1:c.272+175_272+187del	XP_011507836.1:n.272+175_272+187del
XR_921781.1:n.1185+175_1185+187del
XM_011509534.2:c.272+175_272+187del	XP_011507836.1:n.272+175_272+187del
XR_921781.2:n.1183+175_1183+187del
NM_170707.4:c.936+175_936+187del MANE Select	NP_733821.1:n.936+175_936+187del
NM_001257374.3:c.600+175_600+187del	NP_001244303.1:n.600+175_600+187del
NM_001282626.2:c.936+175_936+187del	NP_001269555.1:n.936+175_936+187del
NM_001282624.2:c.693+175_693+187del	NP_001269553.1:n.693+175_693+187del
NM_001282625.2:c.936+175_936+187del	NP_001269554.1:n.936+175_936+187del
NM_005572.4:c.936+175_936+187del MANE Plus Clinical	NP_005563.1:n.936+175_936+187del
NM_170708.4:c.936+175_936+187del	NP_733822.1:n.936+175_936+187del