Canonical Allele Identifier: CA1200471361

Gene: LMNA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156134499_156134500delinsCT , CM000663.2:g.156134499_156134500delinsCT	GRCh38
NC_000001.10:g.156104290_156104291delinsCT , CM000663.1:g.156104290_156104291delinsCT	GRCh37
NC_000001.9:g.154370914_154370915delinsCT	NCBI36
NG_008692.2:g.56927_56928delinsCT , LRG_254:g.56927_56928delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.52_53delinsCT	ENSP00000426535.3:p.Leu18=
ENST00000682650.1:c.610_611delinsCT	ENSP00000506904.1:p.Leu204=
ENST00000683032.1:c.610_611delinsCT	ENSP00000506771.1:p.Leu204=
ENST00000684195.1:c.610_611delinsCT	ENSP00000508220.1:p.Leu204=
ENST00000361308.9:c.610_611delinsCT	ENSP00000355292.6:p.Leu204=
ENST00000368300.9:c.610_611delinsCT MANE Select	ENSP00000357283.4:p.Leu204=
ENST00000496738.6:n.985_986delinsCT
ENST00000504687.6:c.-55_-54delinsCT	ENSP00000426535.2:n.-55_-54delinsCT
ENST00000674518.1:c.610_611delinsCT	ENSP00000502261.1:p.Leu204=
ENST00000674600.1:c.*409_*410delinsCT	ENSP00000501666.1:n.*409_*410delinsCT
ENST00000674720.1:c.610_611delinsCT	ENSP00000502798.1:p.Leu204=
ENST00000675431.1:n.303_304delinsCT
ENST00000675455.1:c.*410_*411delinsCT	ENSP00000501795.1:n.*410_*411delinsCT
ENST00000675667.1:c.610_611delinsCT	ENSP00000501803.1:p.Leu204=
ENST00000675874.1:c.*81_*82delinsCT	ENSP00000501851.1:n.*81_*82delinsCT
ENST00000675881.1:c.610_611delinsCT	ENSP00000501670.1:p.Leu204=
ENST00000675939.1:c.610_611delinsCT	ENSP00000502256.1:p.Leu204=
ENST00000675989.1:n.985_986delinsCT
ENST00000676208.1:c.610_611delinsCT	ENSP00000502468.1:p.Leu204=
ENST00000676283.1:n.985_986delinsCT
ENST00000676385.2:c.610_611delinsCT	ENSP00000502091.1:p.Leu204=
ENST00000676434.1:c.610_611delinsCT	ENSP00000501648.1:p.Leu204=
ENST00000677389.1:c.610_611delinsCT MANE Plus Clinical	ENSP00000503633.1:p.Leu204=
ENST00000347559.6:c.610_611delinsCT	ENSP00000292304.3:p.Leu204=
ENST00000361308.8:c.610_611delinsCT	ENSP00000355292.5:p.Leu204=
ENST00000368297.5:c.367_368delinsCT	ENSP00000357280.1:p.Leu123=
ENST00000368299.7:c.610_611delinsCT	ENSP00000357282.3:p.Leu204=
ENST00000368300.8:c.610_611delinsCT	ENSP00000357283.4:p.Leu204=
ENST00000368301.6:c.610_611delinsCT	ENSP00000357284.2:p.Leu204=
ENST00000448611.6:c.274_275delinsCT	ENSP00000395597.2:p.Leu92=
ENST00000473598.6:c.313_314delinsCT	ENSP00000421821.1:p.Leu105=
ENST00000502357.5:n.508_509delinsCT
ENST00000504687.5:c.361_362delinsCT	ENSP00000426535.1:p.Leu121=
ENST00000515459.5:c.*284_*285delinsCT	ENSP00000424518.1:n.*284_*285delinsCT
NM_001257374.2:c.274_275delinsCT	NP_001244303.1:p.Leu92=
NM_001282624.1:c.367_368delinsCT	NP_001269553.1:p.Leu123=
NM_001282625.1:c.610_611delinsCT	NP_001269554.1:p.Leu204=
NM_001282626.1:c.610_611delinsCT	NP_001269555.1:p.Leu204=
NM_005572.3:c.610_611delinsCT , LRG_254t1:c.610_611delinsCT	NP_005563.1:p.Leu204=
NM_170707.3:c.610_611delinsCT	NP_733821.1:p.Leu204=
NM_170708.3:c.610_611delinsCT	NP_733822.1:p.Leu204=
XM_011509533.1:c.274_275delinsCT	XP_011507835.1:p.Leu92=
XM_011509534.1:c.-55_-54delinsCT	XP_011507836.1:n.-55_-54delinsCT
XR_921781.1:n.859_860delinsCT
XM_011509534.2:c.-55_-54delinsCT	XP_011507836.1:n.-55_-54delinsCT
XR_921781.2:n.857_858delinsCT
NM_170707.4:c.610_611delinsCT MANE Select	NP_733821.1:p.Leu204=
NM_001257374.3:c.274_275delinsCT	NP_001244303.1:p.Leu92=
NM_001282626.2:c.610_611delinsCT	NP_001269555.1:p.Leu204=
NM_001282624.2:c.367_368delinsCT	NP_001269553.1:p.Leu123=
NM_001282625.2:c.610_611delinsCT	NP_001269554.1:p.Leu204=
NM_005572.4:c.610_611delinsCT MANE Plus Clinical	NP_005563.1:p.Leu204=
NM_170708.4:c.610_611delinsCT	NP_733822.1:p.Leu204=