Canonical Allele Identifier: CA1200471147

Gene: LMNA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156134443_156134445delinsATG , CM000663.2:g.156134443_156134445delinsATG	GRCh38
NC_000001.10:g.156104234_156104236delinsATG , CM000663.1:g.156104234_156104236delinsATG	GRCh37
NC_000001.9:g.154370858_154370860delinsATG	NCBI36
NG_008692.2:g.56871_56873delinsATG , LRG_254:g.56871_56873delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.-5_-3delinsATG	ENSP00000426535.3:n.-5_-3delinsATG
ENST00000682650.1:c.554_556delinsATG	ENSP00000506904.1:p.Asp185=
ENST00000683032.1:c.554_556delinsATG	ENSP00000506771.1:p.Asp185=
ENST00000684195.1:c.554_556delinsATG	ENSP00000508220.1:p.Asp185=
ENST00000361308.9:c.554_556delinsATG	ENSP00000355292.6:p.Asp185=
ENST00000368300.9:c.554_556delinsATG MANE Select	ENSP00000357283.4:p.Asp185=
ENST00000496738.6:n.929_931delinsATG
ENST00000504687.6:c.-111_-109delinsATG	ENSP00000426535.2:n.-111_-109delinsATG
ENST00000674518.1:c.554_556delinsATG	ENSP00000502261.1:p.Asp185=
ENST00000674600.1:c.*353_*355delinsATG	ENSP00000501666.1:n.*353_*355delinsATG
ENST00000674720.1:c.554_556delinsATG	ENSP00000502798.1:p.Asp185=
ENST00000675431.1:n.247_249delinsATG
ENST00000675455.1:c.*354_*356delinsATG	ENSP00000501795.1:n.*354_*356delinsATG
ENST00000675667.1:c.554_556delinsATG	ENSP00000501803.1:p.Asp185=
ENST00000675874.1:c.*25_*27delinsATG	ENSP00000501851.1:n.*25_*27delinsATG
ENST00000675881.1:c.554_556delinsATG	ENSP00000501670.1:p.Asp185=
ENST00000675939.1:c.554_556delinsATG	ENSP00000502256.1:p.Asp185=
ENST00000675989.1:n.929_931delinsATG
ENST00000676208.1:c.554_556delinsATG	ENSP00000502468.1:p.Asp185=
ENST00000676283.1:n.929_931delinsATG
ENST00000676385.2:c.554_556delinsATG	ENSP00000502091.1:p.Asp185=
ENST00000676434.1:c.554_556delinsATG	ENSP00000501648.1:p.Asp185=
ENST00000677389.1:c.554_556delinsATG MANE Plus Clinical	ENSP00000503633.1:p.Asp185=
ENST00000347559.6:c.554_556delinsATG	ENSP00000292304.3:p.Asp185=
ENST00000361308.8:c.554_556delinsATG	ENSP00000355292.5:p.Asp185=
ENST00000368297.5:c.311_313delinsATG	ENSP00000357280.1:p.Asp104=
ENST00000368299.7:c.554_556delinsATG	ENSP00000357282.3:p.Asp185=
ENST00000368300.8:c.554_556delinsATG	ENSP00000357283.4:p.Asp185=
ENST00000368301.6:c.554_556delinsATG	ENSP00000357284.2:p.Asp185=
ENST00000448611.6:c.218_220delinsATG	ENSP00000395597.2:p.Asp73=
ENST00000469565.6:n.588_590delinsATG
ENST00000470199.2:n.496_498delinsATG
ENST00000473598.6:c.257_259delinsATG	ENSP00000421821.1:p.Asp86=
ENST00000502357.5:n.452_454delinsATG
ENST00000502751.5:n.526_528delinsATG
ENST00000504687.5:c.305_307delinsATG	ENSP00000426535.1:p.Asp102=
ENST00000515459.5:c.*228_*230delinsATG	ENSP00000424518.1:n.*228_*230delinsATG
NM_001257374.2:c.218_220delinsATG	NP_001244303.1:p.Asp73=
NM_001282624.1:c.311_313delinsATG	NP_001269553.1:p.Asp104=
NM_001282625.1:c.554_556delinsATG	NP_001269554.1:p.Asp185=
NM_001282626.1:c.554_556delinsATG	NP_001269555.1:p.Asp185=
NM_005572.3:c.554_556delinsATG , LRG_254t1:c.554_556delinsATG	NP_005563.1:p.Asp185=
NM_170707.3:c.554_556delinsATG	NP_733821.1:p.Asp185=
NM_170708.3:c.554_556delinsATG	NP_733822.1:p.Asp185=
XM_011509533.1:c.218_220delinsATG	XP_011507835.1:p.Asp73=
XM_011509534.1:c.-111_-109delinsATG	XP_011507836.1:n.-111_-109delinsATG
XR_921781.1:n.803_805delinsATG
XM_011509534.2:c.-111_-109delinsATG	XP_011507836.1:n.-111_-109delinsATG
XR_921781.2:n.801_803delinsATG
NM_170707.4:c.554_556delinsATG MANE Select	NP_733821.1:p.Asp185=
NM_001257374.3:c.218_220delinsATG	NP_001244303.1:p.Asp73=
NM_001282626.2:c.554_556delinsATG	NP_001269555.1:p.Asp185=
NM_001282624.2:c.311_313delinsATG	NP_001269553.1:p.Asp104=
NM_001282625.2:c.554_556delinsATG	NP_001269554.1:p.Asp185=
NM_005572.4:c.554_556delinsATG MANE Plus Clinical	NP_005563.1:p.Asp185=
NM_170708.4:c.554_556delinsATG	NP_733822.1:p.Asp185=