Canonical Allele Identifier: CA2648351939

Gene: LMNA

Linked Data

• gnomAD v4: 1-156137821-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156137825dup , CM000663.2:g.156137825dup	GRCh38
NC_000001.10:g.156107616dup , CM000663.1:g.156107616dup	GRCh37
NC_000001.9:g.154374240dup	NCBI36
NG_008692.2:g.60253dup , LRG_254:g.60253dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.1140+82dup	ENSP00000426535.3:n.1140+82dup
ENST00000498722.3:n.1012dup
ENST00000682650.1:c.1608+593dup	ENSP00000506904.1:n.1608+593dup
ENST00000683032.1:c.1698+82dup	ENSP00000506771.1:n.1698+82dup
ENST00000683773.1:n.43+82dup
ENST00000684195.1:c.*128dup	ENSP00000508220.1:n.*128dup
ENST00000361308.9:c.1698+82dup	ENSP00000355292.6:n.1698+82dup
ENST00000368300.9:c.1698+82dup MANE Select	ENSP00000357283.4:n.1698+82dup
ENST00000496738.6:n.2239dup
ENST00000674518.1:c.*1048+82dup	ENSP00000502261.1:n.*1048+82dup
ENST00000674600.1:c.*1497+82dup	ENSP00000501666.1:n.*1497+82dup
ENST00000674720.1:c.*342dup	ENSP00000502798.1:n.*342dup
ENST00000675431.1:n.1473dup
ENST00000675455.1:c.*1498+82dup	ENSP00000501795.1:n.*1498+82dup
ENST00000675667.1:c.1698+82dup	ENSP00000501803.1:n.1698+82dup
ENST00000675874.1:c.*1169+82dup	ENSP00000501851.1:n.*1169+82dup
ENST00000675881.1:c.*709+82dup	ENSP00000501670.1:n.*709+82dup
ENST00000675939.1:c.1698+82dup	ENSP00000502256.1:n.1698+82dup
ENST00000675989.1:n.2639dup
ENST00000676208.1:c.*801+82dup	ENSP00000502468.1:n.*801+82dup
ENST00000676283.1:n.2576dup
ENST00000676385.2:c.1608+593dup	ENSP00000502091.1:n.1608+593dup
ENST00000676434.1:c.*791dup	ENSP00000501648.1:n.*791dup
ENST00000677389.1:c.*61dup MANE Plus Clinical	ENSP00000503633.1:n.*61dup
ENST00000347559.6:c.1608+593dup	ENSP00000292304.3:n.1608+593dup
ENST00000368297.5:c.*61dup	ENSP00000357280.1:n.*61dup
ENST00000368299.7:c.1698+82dup	ENSP00000357282.3:n.1698+82dup
ENST00000368300.8:c.1698+82dup	ENSP00000357283.4:n.1698+82dup
ENST00000368301.6:c.*61dup	ENSP00000357284.2:n.*61dup
ENST00000448611.6:c.1362+82dup	ENSP00000395597.2:n.1362+82dup
ENST00000473598.6:c.1401+82dup	ENSP00000421821.1:n.1401+82dup
ENST00000496738.5:n.1249dup
ENST00000498722.2:n.1012dup
ENST00000506981.1:n.282+82dup
ENST00000508500.1:c.486+593dup	ENSP00000424977.1:n.486+593dup
NM_001257374.2:c.1362+82dup	NP_001244303.1:n.1362+82dup
NM_001282624.1:c.*61dup	NP_001269553.1:n.*61dup
NM_001282625.1:c.*61dup	NP_001269554.1:n.*61dup
NM_001282626.1:c.1698+82dup	NP_001269555.1:n.1698+82dup
NM_005572.3:c.*61dup , LRG_254t1:c.*61dup	NP_005563.1:n.*61dup
NM_170707.3:c.1698+82dup	NP_733821.1:n.1698+82dup
NM_170708.3:c.1608+593dup	NP_733822.1:n.1608+593dup
XM_011509533.1:c.1362+82dup	XP_011507835.1:n.1362+82dup
XM_011509534.1:c.1074+82dup	XP_011507836.1:n.1074+82dup
XR_921781.1:n.1987+82dup
XM_011509534.2:c.1074+82dup	XP_011507836.1:n.1074+82dup
XR_921781.2:n.1985+82dup
NM_170707.4:c.1698+82dup MANE Select	NP_733821.1:n.1698+82dup
NM_001257374.3:c.1362+82dup	NP_001244303.1:n.1362+82dup
NM_001282626.2:c.1698+82dup	NP_001269555.1:n.1698+82dup
NM_001282624.2:c.*61dup	NP_001269553.1:n.*61dup
NM_001282625.2:c.*61dup	NP_001269554.1:n.*61dup
NM_005572.4:c.*61dup MANE Plus Clinical	NP_005563.1:n.*61dup
NM_170708.4:c.1608+593dup	NP_733822.1:n.1608+593dup