Canonical Allele Identifier: CA2648348806

Gene: LMNA

Linked Data

• gnomAD v4: 1-156135384-TGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156135388_156135389del , CM000663.2:g.156135388_156135389del	GRCh38
NC_000001.10:g.156105179_156105180del , CM000663.1:g.156105179_156105180del	GRCh37
NC_000001.9:g.154371803_154371804del	NCBI36
NG_008692.2:g.57816_57817del , LRG_254:g.57816_57817del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.378+76_378+77del	ENSP00000426535.3:n.378+76_378+77del
ENST00000682650.1:c.936+76_936+77del	ENSP00000506904.1:n.936+76_936+77del
ENST00000683032.1:c.936+76_936+77del	ENSP00000506771.1:n.936+76_936+77del
ENST00000684195.1:c.936+76_936+77del	ENSP00000508220.1:n.936+76_936+77del
ENST00000361308.9:c.936+76_936+77del	ENSP00000355292.6:n.936+76_936+77del
ENST00000368300.9:c.936+76_936+77del MANE Select	ENSP00000357283.4:n.936+76_936+77del
ENST00000496738.6:n.1311+76_1311+77del
ENST00000674518.1:c.*286+76_*286+77del	ENSP00000502261.1:n.*286+76_*286+77del
ENST00000674600.1:c.*735+76_*735+77del	ENSP00000501666.1:n.*735+76_*735+77del
ENST00000674720.1:c.936+76_936+77del	ENSP00000502798.1:n.936+76_936+77del
ENST00000675431.1:n.629+76_629+77del
ENST00000675455.1:c.*736+76_*736+77del	ENSP00000501795.1:n.*736+76_*736+77del
ENST00000675667.1:c.936+76_936+77del	ENSP00000501803.1:n.936+76_936+77del
ENST00000675874.1:c.*407+76_*407+77del	ENSP00000501851.1:n.*407+76_*407+77del
ENST00000675881.1:c.936+76_936+77del	ENSP00000501670.1:n.936+76_936+77del
ENST00000675939.1:c.936+76_936+77del	ENSP00000502256.1:n.936+76_936+77del
ENST00000675989.1:n.1311+76_1311+77del
ENST00000676208.1:c.936+76_936+77del	ENSP00000502468.1:n.936+76_936+77del
ENST00000676283.1:n.1311+76_1311+77del
ENST00000676385.2:c.936+76_936+77del	ENSP00000502091.1:n.936+76_936+77del
ENST00000676434.1:c.936+76_936+77del	ENSP00000501648.1:n.936+76_936+77del
ENST00000677389.1:c.936+76_936+77del MANE Plus Clinical	ENSP00000503633.1:n.936+76_936+77del
ENST00000347559.6:c.936+76_936+77del	ENSP00000292304.3:n.936+76_936+77del
ENST00000361308.8:c.936+76_936+77del	ENSP00000355292.5:n.936+76_936+77del
ENST00000368297.5:c.693+76_693+77del	ENSP00000357280.1:n.693+76_693+77del
ENST00000368298.2:n.200+76_200+77del
ENST00000368299.7:c.936+76_936+77del	ENSP00000357282.3:n.936+76_936+77del
ENST00000368300.8:c.936+76_936+77del	ENSP00000357283.4:n.936+76_936+77del
ENST00000368301.6:c.936+76_936+77del	ENSP00000357284.2:n.936+76_936+77del
ENST00000448611.6:c.600+76_600+77del	ENSP00000395597.2:n.600+76_600+77del
ENST00000473598.6:c.639+76_639+77del	ENSP00000421821.1:n.639+76_639+77del
ENST00000496738.5:n.281+76_281+77del
ENST00000515824.1:n.373_374del
NM_001257374.2:c.600+76_600+77del	NP_001244303.1:n.600+76_600+77del
NM_001282624.1:c.693+76_693+77del	NP_001269553.1:n.693+76_693+77del
NM_001282625.1:c.936+76_936+77del	NP_001269554.1:n.936+76_936+77del
NM_001282626.1:c.936+76_936+77del	NP_001269555.1:n.936+76_936+77del
NM_005572.3:c.936+76_936+77del , LRG_254t1:c.936+76_936+77del	NP_005563.1:n.936+76_936+77del
NM_170707.3:c.936+76_936+77del	NP_733821.1:n.936+76_936+77del
NM_170708.3:c.936+76_936+77del	NP_733822.1:n.936+76_936+77del
XM_011509533.1:c.600+76_600+77del	XP_011507835.1:n.600+76_600+77del
XM_011509534.1:c.272+76_272+77del	XP_011507836.1:n.272+76_272+77del
XR_921781.1:n.1185+76_1185+77del
XM_011509534.2:c.272+76_272+77del	XP_011507836.1:n.272+76_272+77del
XR_921781.2:n.1183+76_1183+77del
NM_170707.4:c.936+76_936+77del MANE Select	NP_733821.1:n.936+76_936+77del
NM_001257374.3:c.600+76_600+77del	NP_001244303.1:n.600+76_600+77del
NM_001282626.2:c.936+76_936+77del	NP_001269555.1:n.936+76_936+77del
NM_001282624.2:c.693+76_693+77del	NP_001269553.1:n.693+76_693+77del
NM_001282625.2:c.936+76_936+77del	NP_001269554.1:n.936+76_936+77del
NM_005572.4:c.936+76_936+77del MANE Plus Clinical	NP_005563.1:n.936+76_936+77del
NM_170708.4:c.936+76_936+77del	NP_733822.1:n.936+76_936+77del