Canonical Allele Identifier: CA1008064952

Gene: LMNA

Linked Data

• dbSNP Id: rs1651587231
• gnomAD v3: 1-156136148-G-GCTGGCAGTGTCCT
• gnomAD v4: 1-156136148-G-GCTGGCAGTGTCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156136154_156136166dup , CM000663.2:g.156136154_156136166dup	GRCh38
NC_000001.10:g.156105945_156105957dup , CM000663.1:g.156105945_156105957dup	GRCh37
NC_000001.9:g.154372569_154372581dup	NCBI36
NG_008692.2:g.58582_58594dup , LRG_254:g.58582_58594dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000504687.7:c.599+33_599+45dup	ENSP00000426535.3:n.599+33_599+45dup
ENST00000498722.3:n.389+33_389+45dup
ENST00000682650.1:c.1157+33_1157+45dup	ENSP00000506904.1:n.1157+33_1157+45dup
ENST00000683032.1:c.1157+33_1157+45dup	ENSP00000506771.1:n.1157+33_1157+45dup
ENST00000684195.1:c.1157+33_1157+45dup	ENSP00000508220.1:n.1157+33_1157+45dup
ENST00000361308.9:c.1157+33_1157+45dup	ENSP00000355292.6:n.1157+33_1157+45dup
ENST00000368300.9:c.1157+33_1157+45dup MANE Select	ENSP00000357283.4:n.1157+33_1157+45dup
ENST00000496738.6:n.1532+33_1532+45dup
ENST00000674518.1:c.*507+33_*507+45dup	ENSP00000502261.1:n.*507+33_*507+45dup
ENST00000674600.1:c.*956+33_*956+45dup	ENSP00000501666.1:n.*956+33_*956+45dup
ENST00000674720.1:c.1157+33_1157+45dup	ENSP00000502798.1:n.1157+33_1157+45dup
ENST00000675431.1:n.850+33_850+45dup
ENST00000675455.1:c.*957+33_*957+45dup	ENSP00000501795.1:n.*957+33_*957+45dup
ENST00000675667.1:c.1157+33_1157+45dup	ENSP00000501803.1:n.1157+33_1157+45dup
ENST00000675874.1:c.*628+33_*628+45dup	ENSP00000501851.1:n.*628+33_*628+45dup
ENST00000675881.1:c.*168+33_*168+45dup	ENSP00000501670.1:n.*168+33_*168+45dup
ENST00000675939.1:c.1157+33_1157+45dup	ENSP00000502256.1:n.1157+33_1157+45dup
ENST00000675989.1:n.1532+33_1532+45dup
ENST00000676208.1:c.*201_*213dup	ENSP00000502468.1:n.*201_*213dup
ENST00000676283.1:n.1532+33_1532+45dup
ENST00000676385.2:c.1157+33_1157+45dup	ENSP00000502091.1:n.1157+33_1157+45dup
ENST00000676434.1:c.*168+33_*168+45dup	ENSP00000501648.1:n.*168+33_*168+45dup
ENST00000677389.1:c.1157+33_1157+45dup MANE Plus Clinical	ENSP00000503633.1:n.1157+33_1157+45dup
ENST00000347559.6:c.1157+33_1157+45dup	ENSP00000292304.3:n.1157+33_1157+45dup
ENST00000361308.8:c.1157+33_1157+45dup	ENSP00000355292.5:n.1157+33_1157+45dup
ENST00000368297.5:c.914+33_914+45dup	ENSP00000357280.1:n.914+33_914+45dup
ENST00000368298.2:n.421+33_421+45dup
ENST00000368299.7:c.1157+33_1157+45dup	ENSP00000357282.3:n.1157+33_1157+45dup
ENST00000368300.8:c.1157+33_1157+45dup	ENSP00000357283.4:n.1157+33_1157+45dup
ENST00000368301.6:c.1157+33_1157+45dup	ENSP00000357284.2:n.1157+33_1157+45dup
ENST00000448611.6:c.821+33_821+45dup	ENSP00000395597.2:n.821+33_821+45dup
ENST00000473598.6:c.860+33_860+45dup	ENSP00000421821.1:n.860+33_860+45dup
ENST00000496738.5:n.542+33_542+45dup
ENST00000498722.2:n.389+33_389+45dup
ENST00000508500.1:c.35+33_35+45dup	ENSP00000424977.1:n.35+33_35+45dup
NM_001257374.2:c.821+33_821+45dup	NP_001244303.1:n.821+33_821+45dup
NM_001282624.1:c.914+33_914+45dup	NP_001269553.1:n.914+33_914+45dup
NM_001282625.1:c.1157+33_1157+45dup	NP_001269554.1:n.1157+33_1157+45dup
NM_001282626.1:c.1157+33_1157+45dup	NP_001269555.1:n.1157+33_1157+45dup
NM_005572.3:c.1157+33_1157+45dup , LRG_254t1:c.1157+33_1157+45dup	NP_005563.1:n.1157+33_1157+45dup
NM_170707.3:c.1157+33_1157+45dup	NP_733821.1:n.1157+33_1157+45dup
NM_170708.3:c.1157+33_1157+45dup	NP_733822.1:n.1157+33_1157+45dup
XM_011509533.1:c.821+33_821+45dup	XP_011507835.1:n.821+33_821+45dup
XM_011509534.1:c.533+33_533+45dup	XP_011507836.1:n.533+33_533+45dup
XR_921781.1:n.1446+33_1446+45dup
XM_011509534.2:c.533+33_533+45dup	XP_011507836.1:n.533+33_533+45dup
XR_921781.2:n.1444+33_1444+45dup
NM_170707.4:c.1157+33_1157+45dup MANE Select	NP_733821.1:n.1157+33_1157+45dup
NM_001257374.3:c.821+33_821+45dup	NP_001244303.1:n.821+33_821+45dup
NM_001282626.2:c.1157+33_1157+45dup	NP_001269555.1:n.1157+33_1157+45dup
NM_001282624.2:c.914+33_914+45dup	NP_001269553.1:n.914+33_914+45dup
NM_001282625.2:c.1157+33_1157+45dup	NP_001269554.1:n.1157+33_1157+45dup
NM_005572.4:c.1157+33_1157+45dup MANE Plus Clinical	NP_005563.1:n.1157+33_1157+45dup
NM_170708.4:c.1157+33_1157+45dup	NP_733822.1:n.1157+33_1157+45dup