Canonical Allele Identifier: CA1200471401

Gene: LMNA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156134508_156134511delinsCAGA , CM000663.2:g.156134508_156134511delinsCAGA	GRCh38
NC_000001.10:g.156104299_156104302delinsCAGA , CM000663.1:g.156104299_156104302delinsCAGA	GRCh37
NC_000001.9:g.154370923_154370926delinsCAGA	NCBI36
NG_008692.2:g.56936_56939delinsCAGA , LRG_254:g.56936_56939delinsCAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.61_64delinsCAGA	ENSP00000426535.3:p.Gln21=
ENST00000682650.1:c.619_622delinsCAGA	ENSP00000506904.1:p.Gln207=
ENST00000683032.1:c.619_622delinsCAGA	ENSP00000506771.1:p.Gln207=
ENST00000684195.1:c.619_622delinsCAGA	ENSP00000508220.1:p.Gln207=
ENST00000361308.9:c.619_622delinsCAGA	ENSP00000355292.6:p.Gln207=
ENST00000368300.9:c.619_622delinsCAGA MANE Select	ENSP00000357283.4:p.Gln207=
ENST00000496738.6:n.994_997delinsCAGA
ENST00000504687.6:c.-46_-43delinsCAGA	ENSP00000426535.2:n.-46_-43delinsCAGA
ENST00000674518.1:c.619_622delinsCAGA	ENSP00000502261.1:p.Gln207=
ENST00000674600.1:c.*418_*421delinsCAGA	ENSP00000501666.1:n.*418_*421delinsCAGA
ENST00000674720.1:c.619_622delinsCAGA	ENSP00000502798.1:p.Gln207=
ENST00000675431.1:n.312_315delinsCAGA
ENST00000675455.1:c.*419_*422delinsCAGA	ENSP00000501795.1:n.*419_*422delinsCAGA
ENST00000675667.1:c.619_622delinsCAGA	ENSP00000501803.1:p.Gln207=
ENST00000675874.1:c.*90_*93delinsCAGA	ENSP00000501851.1:n.*90_*93delinsCAGA
ENST00000675881.1:c.619_622delinsCAGA	ENSP00000501670.1:p.Gln207=
ENST00000675939.1:c.619_622delinsCAGA	ENSP00000502256.1:p.Gln207=
ENST00000675989.1:n.994_997delinsCAGA
ENST00000676208.1:c.619_622delinsCAGA	ENSP00000502468.1:p.Gln207=
ENST00000676283.1:n.994_997delinsCAGA
ENST00000676385.2:c.619_622delinsCAGA	ENSP00000502091.1:p.Gln207=
ENST00000676434.1:c.619_622delinsCAGA	ENSP00000501648.1:p.Gln207=
ENST00000677389.1:c.619_622delinsCAGA MANE Plus Clinical	ENSP00000503633.1:p.Gln207=
ENST00000347559.6:c.619_622delinsCAGA	ENSP00000292304.3:p.Gln207=
ENST00000361308.8:c.619_622delinsCAGA	ENSP00000355292.5:p.Gln207=
ENST00000368297.5:c.376_379delinsCAGA	ENSP00000357280.1:p.Gln126=
ENST00000368299.7:c.619_622delinsCAGA	ENSP00000357282.3:p.Gln207=
ENST00000368300.8:c.619_622delinsCAGA	ENSP00000357283.4:p.Gln207=
ENST00000368301.6:c.619_622delinsCAGA	ENSP00000357284.2:p.Gln207=
ENST00000448611.6:c.283_286delinsCAGA	ENSP00000395597.2:p.Gln95=
ENST00000473598.6:c.322_325delinsCAGA	ENSP00000421821.1:p.Gln108=
ENST00000502357.5:n.517_520delinsCAGA
ENST00000504687.5:c.370_373delinsCAGA	ENSP00000426535.1:p.Gln124=
ENST00000515459.5:c.*293_*296delinsCAGA	ENSP00000424518.1:n.*293_*296delinsCAGA
NM_001257374.2:c.283_286delinsCAGA	NP_001244303.1:p.Gln95=
NM_001282624.1:c.376_379delinsCAGA	NP_001269553.1:p.Gln126=
NM_001282625.1:c.619_622delinsCAGA	NP_001269554.1:p.Gln207=
NM_001282626.1:c.619_622delinsCAGA	NP_001269555.1:p.Gln207=
NM_005572.3:c.619_622delinsCAGA , LRG_254t1:c.619_622delinsCAGA	NP_005563.1:p.Gln207=
NM_170707.3:c.619_622delinsCAGA	NP_733821.1:p.Gln207=
NM_170708.3:c.619_622delinsCAGA	NP_733822.1:p.Gln207=
XM_011509533.1:c.283_286delinsCAGA	XP_011507835.1:p.Gln95=
XM_011509534.1:c.-46_-43delinsCAGA	XP_011507836.1:n.-46_-43delinsCAGA
XR_921781.1:n.868_871delinsCAGA
XM_011509534.2:c.-46_-43delinsCAGA	XP_011507836.1:n.-46_-43delinsCAGA
XR_921781.2:n.866_869delinsCAGA
NM_170707.4:c.619_622delinsCAGA MANE Select	NP_733821.1:p.Gln207=
NM_001257374.3:c.283_286delinsCAGA	NP_001244303.1:p.Gln95=
NM_001282626.2:c.619_622delinsCAGA	NP_001269555.1:p.Gln207=
NM_001282624.2:c.376_379delinsCAGA	NP_001269553.1:p.Gln126=
NM_001282625.2:c.619_622delinsCAGA	NP_001269554.1:p.Gln207=
NM_005572.4:c.619_622delinsCAGA MANE Plus Clinical	NP_005563.1:p.Gln207=
NM_170708.4:c.619_622delinsCAGA	NP_733822.1:p.Gln207=