Canonical Allele Identifier: CA342825590

Gene: LMNA

Linked Data

• MyVariant Identifiers: chr1:g.156107494A>T (hg19) ; chr1:g.156137703A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156137703A>T , CM000663.2:g.156137703A>T	GRCh38
NC_000001.10:g.156107494A>T , CM000663.1:g.156107494A>T	GRCh37
NC_000001.9:g.154374118A>T	NCBI36
NG_008692.2:g.60131A>T , LRG_254:g.60131A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.1100A>T	ENSP00000426535.3:p.Asp367Val
ENST00000498722.3:n.890A>T
ENST00000682650.1:c.1608+471A>T	ENSP00000506904.1:n.1608+471A>T
ENST00000683032.1:c.1658A>T	ENSP00000506771.1:p.Asp553Val
ENST00000683773.1:n.3A>T
ENST00000684195.1:c.*6A>T	ENSP00000508220.1:n.*6A>T
ENST00000361308.9:c.1658A>T	ENSP00000355292.6:p.Asp553Val
ENST00000368300.9:c.1658A>T MANE Select	ENSP00000357283.4:p.Asp553Val
ENST00000496738.6:n.2117A>T
ENST00000674518.1:c.*1008A>T	ENSP00000502261.1:n.*1008A>T
ENST00000674600.1:c.*1457A>T	ENSP00000501666.1:n.*1457A>T
ENST00000674720.1:c.*220A>T	ENSP00000502798.1:n.*220A>T
ENST00000675431.1:n.1351A>T
ENST00000675455.1:c.*1458A>T	ENSP00000501795.1:n.*1458A>T
ENST00000675667.1:c.1658A>T	ENSP00000501803.1:p.Asp553Val
ENST00000675874.1:c.*1129A>T	ENSP00000501851.1:n.*1129A>T
ENST00000675881.1:c.*669A>T	ENSP00000501670.1:n.*669A>T
ENST00000675939.1:c.1658A>T	ENSP00000502256.1:p.Asp553Val
ENST00000675989.1:n.2517A>T
ENST00000676208.1:c.*761A>T	ENSP00000502468.1:n.*761A>T
ENST00000676283.1:n.2454A>T
ENST00000676385.2:c.1608+471A>T	ENSP00000502091.1:n.1608+471A>T
ENST00000676434.1:c.*669A>T	ENSP00000501648.1:n.*669A>T
ENST00000677389.1:c.1658A>T MANE Plus Clinical	ENSP00000503633.1:p.Asp553Val
ENST00000347559.6:c.1608+471A>T	ENSP00000292304.3:n.1608+471A>T
ENST00000361308.8:c.1403A>T	ENSP00000355292.5:p.Asp468Val
ENST00000368297.5:c.1415A>T	ENSP00000357280.1:p.Asp472Val
ENST00000368299.7:c.1658A>T	ENSP00000357282.3:p.Asp553Val
ENST00000368300.8:c.1658A>T	ENSP00000357283.4:p.Asp553Val
ENST00000368301.6:c.1658A>T	ENSP00000357284.2:p.Asp553Val
ENST00000448611.6:c.1322A>T	ENSP00000395597.2:p.Asp441Val
ENST00000473598.6:c.1361A>T	ENSP00000421821.1:p.Asp454Val
ENST00000496738.5:n.1127A>T
ENST00000498722.2:n.890A>T
ENST00000506981.1:n.242A>T
ENST00000508500.1:c.486+471A>T	ENSP00000424977.1:n.486+471A>T
NM_001257374.2:c.1322A>T	NP_001244303.1:p.Asp441Val
NM_001282624.1:c.1415A>T	NP_001269553.1:p.Asp472Val
NM_001282625.1:c.1658A>T	NP_001269554.1:p.Asp553Val
NM_001282626.1:c.1658A>T	NP_001269555.1:p.Asp553Val
NM_005572.3:c.1658A>T , LRG_254t1:c.1658A>T	NP_005563.1:p.Asp553Val
NM_170707.3:c.1658A>T	NP_733821.1:p.Asp553Val
NM_170708.3:c.1608+471A>T	NP_733822.1:n.1608+471A>T
XM_011509533.1:c.1322A>T	XP_011507835.1:p.Asp441Val
XM_011509534.1:c.1034A>T	XP_011507836.1:p.Asp345Val
XR_921781.1:n.1947A>T
XM_011509534.2:c.1034A>T	XP_011507836.1:p.Asp345Val
XR_921781.2:n.1945A>T
NM_170707.4:c.1658A>T MANE Select	NP_733821.1:p.Asp553Val
NM_001257374.3:c.1322A>T	NP_001244303.1:p.Asp441Val
NM_001282626.2:c.1658A>T	NP_001269555.1:p.Asp553Val
NM_001282624.2:c.1415A>T	NP_001269553.1:p.Asp472Val
NM_001282625.2:c.1658A>T	NP_001269554.1:p.Asp553Val
NM_005572.4:c.1658A>T MANE Plus Clinical	NP_005563.1:p.Asp553Val
NM_170708.4:c.1608+471A>T	NP_733822.1:n.1608+471A>T