Canonical Allele Identifier: CA2697457959

Gene: LMNA

Linked Data

• dbSNP Id: rs2102897312

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156137520del , CM000663.2:g.156137520del	GRCh38
NC_000001.10:g.156107311del , CM000663.1:g.156107311del	GRCh37
NC_000001.9:g.154373935del	NCBI36
NG_008692.2:g.59948del , LRG_254:g.59948del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.1051-134del	ENSP00000426535.3:n.1051-134del
ENST00000498722.3:n.841-134del
ENST00000682650.1:c.1608+288del	ENSP00000506904.1:n.1608+288del
ENST00000683032.1:c.1609-134del	ENSP00000506771.1:n.1609-134del
ENST00000684195.1:c.1580-134del	ENSP00000508220.1:n.1580-134del
ENST00000361308.9:c.1609-134del	ENSP00000355292.6:n.1609-134del
ENST00000368300.9:c.1609-134del MANE Select	ENSP00000357283.4:n.1609-134del
ENST00000496738.6:n.2068-134del
ENST00000674518.1:c.*959-134del	ENSP00000502261.1:n.*959-134del
ENST00000674600.1:c.*1408-134del	ENSP00000501666.1:n.*1408-134del
ENST00000674720.1:c.*171-134del	ENSP00000502798.1:n.*171-134del
ENST00000675431.1:n.1302-134del
ENST00000675455.1:c.*1409-134del	ENSP00000501795.1:n.*1409-134del
ENST00000675667.1:c.1609-134del	ENSP00000501803.1:n.1609-134del
ENST00000675874.1:c.*1080-134del	ENSP00000501851.1:n.*1080-134del
ENST00000675881.1:c.*620-134del	ENSP00000501670.1:n.*620-134del
ENST00000675939.1:c.1609-134del	ENSP00000502256.1:n.1609-134del
ENST00000675989.1:n.2468-134del
ENST00000676208.1:c.*712-134del	ENSP00000502468.1:n.*712-134del
ENST00000676283.1:n.2271del
ENST00000676385.2:c.1608+288del	ENSP00000502091.1:n.1608+288del
ENST00000676434.1:c.*620-134del	ENSP00000501648.1:n.*620-134del
ENST00000677389.1:c.1609-134del MANE Plus Clinical	ENSP00000503633.1:n.1609-134del
ENST00000347559.6:c.1608+288del	ENSP00000292304.3:n.1608+288del
ENST00000361308.8:c.1354-134del	ENSP00000355292.5:n.1354-134del
ENST00000368297.5:c.1366-134del	ENSP00000357280.1:n.1366-134del
ENST00000368299.7:c.1609-134del	ENSP00000357282.3:n.1609-134del
ENST00000368300.8:c.1609-134del	ENSP00000357283.4:n.1609-134del
ENST00000368301.6:c.1609-134del	ENSP00000357284.2:n.1609-134del
ENST00000448611.6:c.1273-134del	ENSP00000395597.2:n.1273-134del
ENST00000473598.6:c.1312-134del	ENSP00000421821.1:n.1312-134del
ENST00000496738.5:n.1078-134del
ENST00000498722.2:n.841-134del
ENST00000506981.1:n.59del
ENST00000508500.1:c.486+288del	ENSP00000424977.1:n.486+288del
NM_001257374.2:c.1273-134del	NP_001244303.1:n.1273-134del
NM_001282624.1:c.1366-134del	NP_001269553.1:n.1366-134del
NM_001282625.1:c.1609-134del	NP_001269554.1:n.1609-134del
NM_001282626.1:c.1609-134del	NP_001269555.1:n.1609-134del
NM_005572.3:c.1609-134del , LRG_254t1:c.1609-134del	NP_005563.1:n.1609-134del
NM_170707.3:c.1609-134del	NP_733821.1:n.1609-134del
NM_170708.3:c.1608+288del	NP_733822.1:n.1608+288del
XM_011509533.1:c.1273-134del	XP_011507835.1:n.1273-134del
XM_011509534.1:c.985-134del	XP_011507836.1:n.985-134del
XR_921781.1:n.1898-134del
XM_011509534.2:c.985-134del	XP_011507836.1:n.985-134del
XR_921781.2:n.1896-134del
NM_170707.4:c.1609-134del MANE Select	NP_733821.1:n.1609-134del
NM_001257374.3:c.1273-134del	NP_001244303.1:n.1273-134del
NM_001282626.2:c.1609-134del	NP_001269555.1:n.1609-134del
NM_001282624.2:c.1366-134del	NP_001269553.1:n.1366-134del
NM_001282625.2:c.1609-134del	NP_001269554.1:n.1609-134del
NM_005572.4:c.1609-134del MANE Plus Clinical	NP_005563.1:n.1609-134del
NM_170708.4:c.1608+288del	NP_733822.1:n.1608+288del