Canonical Allele Identifier: CA1200467987

Gene: LMNA

Linked Data

• dbSNP Id: rs1650993860

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156130786T>G , CM000663.2:g.156130786T>G	GRCh38
NC_000001.10:g.156100577T>G , CM000663.1:g.156100577T>G	GRCh37
NC_000001.9:g.154367201T>G	NCBI36
NG_008692.2:g.53214T>G , LRG_254:g.53214T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.-46+13T>G	ENSP00000426535.3:n.-46+13T>G
ENST00000682650.1:c.513+13T>G	ENSP00000506904.1:n.513+13T>G
ENST00000683032.1:c.513+13T>G	ENSP00000506771.1:n.513+13T>G
ENST00000684195.1:c.513+13T>G	ENSP00000508220.1:n.513+13T>G
ENST00000361308.9:c.513+13T>G	ENSP00000355292.6:n.513+13T>G
ENST00000368300.9:c.513+13T>G MANE Select	ENSP00000357283.4:n.513+13T>G
ENST00000496738.6:n.888+13T>G
ENST00000504687.6:c.-152+13T>G	ENSP00000426535.2:n.-152+13T>G
ENST00000674518.1:c.513+13T>G	ENSP00000502261.1:n.513+13T>G
ENST00000674600.1:c.*312+13T>G	ENSP00000501666.1:n.*312+13T>G
ENST00000674720.1:c.513+13T>G	ENSP00000502798.1:n.513+13T>G
ENST00000675431.1:n.206+13T>G
ENST00000675455.1:c.*313+13T>G	ENSP00000501795.1:n.*313+13T>G
ENST00000675667.1:c.513+13T>G	ENSP00000501803.1:n.513+13T>G
ENST00000675874.1:c.357-3617T>G	ENSP00000501851.1:n.357-3617T>G
ENST00000675881.1:c.513+13T>G	ENSP00000501670.1:n.513+13T>G
ENST00000675939.1:c.513+13T>G	ENSP00000502256.1:n.513+13T>G
ENST00000675989.1:n.888+13T>G
ENST00000676208.1:c.513+13T>G	ENSP00000502468.1:n.513+13T>G
ENST00000676283.1:n.888+13T>G
ENST00000676385.2:c.513+13T>G	ENSP00000502091.1:n.513+13T>G
ENST00000676434.1:c.513+13T>G	ENSP00000501648.1:n.513+13T>G
ENST00000677389.1:c.513+13T>G MANE Plus Clinical	ENSP00000503633.1:n.513+13T>G
ENST00000347559.6:c.513+13T>G	ENSP00000292304.3:n.513+13T>G
ENST00000361308.8:c.513+13T>G	ENSP00000355292.5:n.513+13T>G
ENST00000368297.5:c.270+13T>G	ENSP00000357280.1:n.270+13T>G
ENST00000368299.7:c.513+13T>G	ENSP00000357282.3:n.513+13T>G
ENST00000368300.8:c.513+13T>G	ENSP00000357283.4:n.513+13T>G
ENST00000368301.6:c.513+13T>G	ENSP00000357284.2:n.513+13T>G
ENST00000448611.6:c.177+13T>G	ENSP00000395597.2:n.177+13T>G
ENST00000469565.6:n.547+13T>G
ENST00000470199.2:n.455+13T>G
ENST00000473598.6:c.216+13T>G	ENSP00000421821.1:n.216+13T>G
ENST00000502357.5:n.411+13T>G
ENST00000502751.5:n.485+13T>G
ENST00000504687.5:c.264+13T>G	ENSP00000426535.1:n.264+13T>G
ENST00000515459.5:c.*187+13T>G	ENSP00000424518.1:n.*187+13T>G
NM_001257374.2:c.177+13T>G	NP_001244303.1:n.177+13T>G
NM_001282624.1:c.270+13T>G	NP_001269553.1:n.270+13T>G
NM_001282625.1:c.513+13T>G	NP_001269554.1:n.513+13T>G
NM_001282626.1:c.513+13T>G	NP_001269555.1:n.513+13T>G
NM_005572.3:c.513+13T>G , LRG_254t1:c.513+13T>G	NP_005563.1:n.513+13T>G
NM_170707.3:c.513+13T>G	NP_733821.1:n.513+13T>G
NM_170708.3:c.513+13T>G	NP_733822.1:n.513+13T>G
XM_011509533.1:c.177+13T>G	XP_011507835.1:n.177+13T>G
XM_011509534.1:c.-152+13T>G	XP_011507836.1:n.-152+13T>G
XR_921781.1:n.762+13T>G
XM_011509534.2:c.-152+13T>G	XP_011507836.1:n.-152+13T>G
XR_921781.2:n.760+13T>G
NM_170707.4:c.513+13T>G MANE Select	NP_733821.1:n.513+13T>G
NM_001257374.3:c.177+13T>G	NP_001244303.1:n.177+13T>G
NM_001282626.2:c.513+13T>G	NP_001269555.1:n.513+13T>G
NM_001282624.2:c.270+13T>G	NP_001269553.1:n.270+13T>G
NM_001282625.2:c.513+13T>G	NP_001269554.1:n.513+13T>G
NM_005572.4:c.513+13T>G MANE Plus Clinical	NP_005563.1:n.513+13T>G
NM_170708.4:c.513+13T>G	NP_733822.1:n.513+13T>G