Canonical Allele Identifier: CA2586964224

Gene: LMNA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156136229dup , CM000663.2:g.156136229dup	GRCh38
NC_000001.10:g.156106020dup , CM000663.1:g.156106020dup	GRCh37
NC_000001.9:g.154372644dup	NCBI36
NG_008692.2:g.58657dup , LRG_254:g.58657dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.615dup	ENSP00000426535.3:p.Ser206GlnfsTer?
ENST00000498722.3:n.405dup
ENST00000682650.1:c.1173dup	ENSP00000506904.1:p.Ser392GlnfsTer?
ENST00000683032.1:c.1173dup	ENSP00000506771.1:p.Ser392GlnfsTer?
ENST00000684195.1:c.1173dup	ENSP00000508220.1:p.Ser392GlnfsTer?
ENST00000361308.9:c.1173dup	ENSP00000355292.6:p.Ser392GlnfsTer?
ENST00000368300.9:c.1173dup MANE Select	ENSP00000357283.4:p.Ser392GlnfsTer?
ENST00000496738.6:n.1548dup
ENST00000674518.1:c.*523dup	ENSP00000502261.1:n.*523dup
ENST00000674600.1:c.*972dup	ENSP00000501666.1:n.*972dup
ENST00000674720.1:c.1173dup	ENSP00000502798.1:p.Ser392GlnfsTer?
ENST00000675431.1:n.866dup
ENST00000675455.1:c.*973dup	ENSP00000501795.1:n.*973dup
ENST00000675667.1:c.1173dup	ENSP00000501803.1:p.Ser392GlnfsTer?
ENST00000675874.1:c.*644dup	ENSP00000501851.1:n.*644dup
ENST00000675881.1:c.*184dup	ENSP00000501670.1:n.*184dup
ENST00000675939.1:c.1173dup	ENSP00000502256.1:p.Ser392GlnfsTer?
ENST00000675989.1:n.1548dup
ENST00000676208.1:c.*276dup	ENSP00000502468.1:n.*276dup
ENST00000676283.1:n.1548dup
ENST00000676385.2:c.1173dup	ENSP00000502091.1:p.Ser392GlnfsTer?
ENST00000676434.1:c.*184dup	ENSP00000501648.1:n.*184dup
ENST00000677389.1:c.1173dup MANE Plus Clinical	ENSP00000503633.1:p.Ser392GlnfsTer?
ENST00000347559.6:c.1173dup	ENSP00000292304.3:p.Ser392GlnfsTer?
ENST00000361308.8:c.1173dup	ENSP00000355292.5:p.Ser392GlnfsTer?
ENST00000368297.5:c.930dup	ENSP00000357280.1:p.Ser311GlnfsTer?
ENST00000368298.2:n.437dup
ENST00000368299.7:c.1173dup	ENSP00000357282.3:p.Ser392GlnfsTer?
ENST00000368300.8:c.1173dup	ENSP00000357283.4:p.Ser392GlnfsTer?
ENST00000368301.6:c.1173dup	ENSP00000357284.2:p.Ser392GlnfsTer?
ENST00000448611.6:c.837dup	ENSP00000395597.2:p.Ser280GlnfsTer?
ENST00000473598.6:c.876dup	ENSP00000421821.1:p.Ser293GlnfsTer?
ENST00000496738.5:n.558dup
ENST00000498722.2:n.405dup
ENST00000508500.1:c.51dup	ENSP00000424977.1:p.Ser18GlnfsTer?
NM_001257374.2:c.837dup	NP_001244303.1:p.Ser280GlnfsTer?
NM_001282624.1:c.930dup	NP_001269553.1:p.Ser311GlnfsTer?
NM_001282625.1:c.1173dup	NP_001269554.1:p.Ser392GlnfsTer?
NM_001282626.1:c.1173dup	NP_001269555.1:p.Ser392GlnfsTer?
NM_005572.3:c.1173dup , LRG_254t1:c.1173dup	NP_005563.1:p.Ser392GlnfsTer?
NM_170707.3:c.1173dup	NP_733821.1:p.Ser392GlnfsTer?
NM_170708.3:c.1173dup	NP_733822.1:p.Ser392GlnfsTer?
XM_011509533.1:c.837dup	XP_011507835.1:p.Ser280GlnfsTer?
XM_011509534.1:c.549dup	XP_011507836.1:p.Ser184GlnfsTer?
XR_921781.1:n.1462dup
XM_011509534.2:c.549dup	XP_011507836.1:p.Ser184GlnfsTer?
XR_921781.2:n.1460dup
NM_170707.4:c.1173dup MANE Select	NP_733821.1:p.Ser392GlnfsTer?
NM_001257374.3:c.837dup	NP_001244303.1:p.Ser280GlnfsTer?
NM_001282626.2:c.1173dup	NP_001269555.1:p.Ser392GlnfsTer?
NM_001282624.2:c.930dup	NP_001269553.1:p.Ser311GlnfsTer?
NM_001282625.2:c.1173dup	NP_001269554.1:p.Ser392GlnfsTer?
NM_005572.4:c.1173dup MANE Plus Clinical	NP_005563.1:p.Ser392GlnfsTer?
NM_170708.4:c.1173dup	NP_733822.1:p.Ser392GlnfsTer?