Canonical Allele Identifier: CA421069080

Gene: LMNA

Linked Data

• MyVariant Identifiers: chr1:g.156106906C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156137115C>T , CM000663.2:g.156137115C>T	GRCh38
NC_000001.10:g.156106906C>T , CM000663.1:g.156106906C>T	GRCh37
NC_000001.9:g.154373530C>T	NCBI36
NG_008692.2:g.59543C>T , LRG_254:g.59543C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000504687.7:c.933C>T	ENSP00000426535.3:p.Ile311=
ENST00000459904.2:n.739C>T
ENST00000498722.3:n.723C>T
ENST00000682650.1:c.1491C>T	ENSP00000506904.1:p.Ile497=
ENST00000683032.1:c.1491C>T	ENSP00000506771.1:p.Ile497=
ENST00000684195.1:c.1491C>T	ENSP00000508220.1:p.Ile497=
ENST00000361308.9:c.1491C>T	ENSP00000355292.6:p.Ile497=
ENST00000368300.9:c.1491C>T MANE Select	ENSP00000357283.4:p.Ile497=
ENST00000496738.6:n.1950C>T
ENST00000674518.1:c.*841C>T	ENSP00000502261.1:n.*841C>T
ENST00000674600.1:c.*1290C>T	ENSP00000501666.1:n.*1290C>T
ENST00000674720.1:c.*53C>T	ENSP00000502798.1:n.*53C>T
ENST00000675431.1:n.1184C>T
ENST00000675455.1:c.*1291C>T	ENSP00000501795.1:n.*1291C>T
ENST00000675667.1:c.1491C>T	ENSP00000501803.1:p.Ile497=
ENST00000675874.1:c.*962C>T	ENSP00000501851.1:n.*962C>T
ENST00000675881.1:c.*502C>T	ENSP00000501670.1:n.*502C>T
ENST00000675939.1:c.1491C>T	ENSP00000502256.1:p.Ile497=
ENST00000675989.1:n.2350C>T
ENST00000676208.1:c.*594C>T	ENSP00000502468.1:n.*594C>T
ENST00000676283.1:n.1866C>T
ENST00000676385.2:c.1491C>T	ENSP00000502091.1:p.Ile497=
ENST00000676434.1:c.*502C>T	ENSP00000501648.1:n.*502C>T
ENST00000677389.1:c.1491C>T MANE Plus Clinical	ENSP00000503633.1:p.Ile497=
ENST00000347559.6:c.1491C>T	ENSP00000292304.3:p.Ile497=
ENST00000361308.8:c.1312-76C>T	ENSP00000355292.5:n.1312-76C>T
ENST00000368297.5:c.1248C>T	ENSP00000357280.1:p.Ile416=
ENST00000368298.2:n.1323C>T
ENST00000368299.7:c.1491C>T	ENSP00000357282.3:p.Ile497=
ENST00000368300.8:c.1491C>T	ENSP00000357283.4:p.Ile497=
ENST00000368301.6:c.1491C>T	ENSP00000357284.2:p.Ile497=
ENST00000448611.6:c.1155C>T	ENSP00000395597.2:p.Ile385=
ENST00000459904.1:n.739C>T
ENST00000473598.6:c.1194C>T	ENSP00000421821.1:p.Ile398=
ENST00000496738.5:n.960C>T
ENST00000498722.2:n.723C>T
ENST00000508500.1:c.369C>T	ENSP00000424977.1:p.Ile123=
NM_001257374.2:c.1155C>T	NP_001244303.1:p.Ile385=
NM_001282624.1:c.1248C>T	NP_001269553.1:p.Ile416=
NM_001282625.1:c.1491C>T	NP_001269554.1:p.Ile497=
NM_001282626.1:c.1491C>T	NP_001269555.1:p.Ile497=
NM_005572.3:c.1491C>T , LRG_254t1:c.1491C>T	NP_005563.1:p.Ile497=
NM_170707.3:c.1491C>T	NP_733821.1:p.Ile497=
NM_170708.3:c.1491C>T	NP_733822.1:p.Ile497=
XM_011509533.1:c.1155C>T	XP_011507835.1:p.Ile385=
XM_011509534.1:c.867C>T	XP_011507836.1:p.Ile289=
XR_921781.1:n.1780C>T
XM_011509534.2:c.867C>T	XP_011507836.1:p.Ile289=
XR_921781.2:n.1778C>T
NM_170707.4:c.1491C>T MANE Select	NP_733821.1:p.Ile497=
NM_001257374.3:c.1155C>T	NP_001244303.1:p.Ile385=
NM_001282626.2:c.1491C>T	NP_001269555.1:p.Ile497=
NM_001282624.2:c.1248C>T	NP_001269553.1:p.Ile416=
NM_001282625.2:c.1491C>T	NP_001269554.1:p.Ile497=
NM_005572.4:c.1491C>T MANE Plus Clinical	NP_005563.1:p.Ile497=
NM_170708.4:c.1491C>T	NP_733822.1:p.Ile497=