Canonical Allele Identifier: CA342817301

Gene: LMNA

Linked Data

• MyVariant Identifiers: chr1:g.156104695G>C (hg19) ; chr1:g.156134904G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156134904G>C , CM000663.2:g.156134904G>C	GRCh38
NC_000001.10:g.156104695G>C , CM000663.1:g.156104695G>C	GRCh37
NC_000001.9:g.154371319G>C	NCBI36
NG_008692.2:g.57332G>C , LRG_254:g.57332G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000504687.7:c.181G>C	ENSP00000426535.3:p.Glu61Gln
ENST00000682650.1:c.739G>C	ENSP00000506904.1:p.Glu247Gln
ENST00000683032.1:c.739G>C	ENSP00000506771.1:p.Glu247Gln
ENST00000684195.1:c.739G>C	ENSP00000508220.1:p.Glu247Gln
ENST00000361308.9:c.739G>C	ENSP00000355292.6:p.Glu247Gln
ENST00000368300.9:c.739G>C MANE Select	ENSP00000357283.4:p.Glu247Gln
ENST00000496738.6:n.1114G>C
ENST00000504687.6:c.75G>C	ENSP00000426535.2:p.Arg25Ser
ENST00000674518.1:c.*89G>C	ENSP00000502261.1:n.*89G>C
ENST00000674600.1:c.*538G>C	ENSP00000501666.1:n.*538G>C
ENST00000674720.1:c.739G>C	ENSP00000502798.1:p.Glu247Gln
ENST00000675431.1:n.432G>C
ENST00000675455.1:c.*539G>C	ENSP00000501795.1:n.*539G>C
ENST00000675667.1:c.739G>C	ENSP00000501803.1:p.Glu247Gln
ENST00000675874.1:c.*210G>C	ENSP00000501851.1:n.*210G>C
ENST00000675881.1:c.739G>C	ENSP00000501670.1:p.Glu247Gln
ENST00000675939.1:c.739G>C	ENSP00000502256.1:p.Glu247Gln
ENST00000675989.1:n.1114G>C
ENST00000676208.1:c.739G>C	ENSP00000502468.1:p.Glu247Gln
ENST00000676283.1:n.1114G>C
ENST00000676385.2:c.739G>C	ENSP00000502091.1:p.Glu247Gln
ENST00000676434.1:c.739G>C	ENSP00000501648.1:p.Glu247Gln
ENST00000677389.1:c.739G>C MANE Plus Clinical	ENSP00000503633.1:p.Glu247Gln
ENST00000347559.6:c.739G>C	ENSP00000292304.3:p.Glu247Gln
ENST00000361308.8:c.739G>C	ENSP00000355292.5:p.Glu247Gln
ENST00000368297.5:c.496G>C	ENSP00000357280.1:p.Glu166Gln
ENST00000368299.7:c.739G>C	ENSP00000357282.3:p.Glu247Gln
ENST00000368300.8:c.739G>C	ENSP00000357283.4:p.Glu247Gln
ENST00000368301.6:c.739G>C	ENSP00000357284.2:p.Glu247Gln
ENST00000448611.6:c.403G>C	ENSP00000395597.2:p.Glu135Gln
ENST00000473598.6:c.442G>C	ENSP00000421821.1:p.Glu148Gln
ENST00000496738.5:n.84G>C
ENST00000504687.5:c.490G>C	ENSP00000426535.1:p.Glu164Gln
ENST00000515459.5:c.*413G>C	ENSP00000424518.1:n.*413G>C
ENST00000515824.1:n.100G>C
NM_001257374.2:c.403G>C	NP_001244303.1:p.Glu135Gln
NM_001282624.1:c.496G>C	NP_001269553.1:p.Glu166Gln
NM_001282625.1:c.739G>C	NP_001269554.1:p.Glu247Gln
NM_001282626.1:c.739G>C	NP_001269555.1:p.Glu247Gln
NM_005572.3:c.739G>C , LRG_254t1:c.739G>C	NP_005563.1:p.Glu247Gln
NM_170707.3:c.739G>C	NP_733821.1:p.Glu247Gln
NM_170708.3:c.739G>C	NP_733822.1:p.Glu247Gln
XM_011509533.1:c.403G>C	XP_011507835.1:p.Glu135Gln
XM_011509534.1:c.75G>C	XP_011507836.1:p.Arg25Ser
XR_921781.1:n.988G>C
XM_011509534.2:c.75G>C	XP_011507836.1:p.Arg25Ser
XR_921781.2:n.986G>C
NM_170707.4:c.739G>C MANE Select	NP_733821.1:p.Glu247Gln
NM_001257374.3:c.403G>C	NP_001244303.1:p.Glu135Gln
NM_001282626.2:c.739G>C	NP_001269555.1:p.Glu247Gln
NM_001282624.2:c.496G>C	NP_001269553.1:p.Glu166Gln
NM_001282625.2:c.739G>C	NP_001269554.1:p.Glu247Gln
NM_005572.4:c.739G>C MANE Plus Clinical	NP_005563.1:p.Glu247Gln
NM_170708.4:c.739G>C	NP_733822.1:p.Glu247Gln