Canonical Allele Identifier: CA421257898

Gene: LMNA

Linked Data

• MyVariant Identifiers: chr1:g.156108326C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156138535C>A , CM000663.2:g.156138535C>A	GRCh38
NC_000001.10:g.156108326C>A , CM000663.1:g.156108326C>A	GRCh37
NC_000001.9:g.154374950C>A	NCBI36
NG_008692.2:g.60963C>A , LRG_254:g.60963C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.1188C>A	ENSP00000426535.3:p.Arg396=
ENST00000682650.1:c.1656C>A	ENSP00000506904.1:p.Arg552=
ENST00000683032.1:c.1746C>A	ENSP00000506771.1:p.Arg582=
ENST00000683773.1:n.91C>A
ENST00000684195.1:c.*838C>A	ENSP00000508220.1:n.*838C>A
ENST00000361308.9:c.1746C>A	ENSP00000355292.6:p.Arg582=
ENST00000368300.9:c.1746C>A MANE Select	ENSP00000357283.4:p.Arg582=
ENST00000496738.6:n.2949C>A
ENST00000674518.1:c.*1096C>A	ENSP00000502261.1:n.*1096C>A
ENST00000674600.1:c.*1545C>A	ENSP00000501666.1:n.*1545C>A
ENST00000674720.1:c.*1052C>A	ENSP00000502798.1:n.*1052C>A
ENST00000675455.1:c.*1546C>A	ENSP00000501795.1:n.*1546C>A
ENST00000675667.1:c.1746C>A	ENSP00000501803.1:p.Arg582=
ENST00000675874.1:c.*1217C>A	ENSP00000501851.1:n.*1217C>A
ENST00000675881.1:c.*757C>A	ENSP00000501670.1:n.*757C>A
ENST00000675939.1:c.1746C>A	ENSP00000502256.1:p.Arg582=
ENST00000675989.1:n.3349C>A
ENST00000676208.1:c.*849C>A	ENSP00000502468.1:n.*849C>A
ENST00000676283.1:n.3286C>A
ENST00000676385.2:c.1656C>A	ENSP00000502091.1:p.Arg552=
ENST00000676434.1:c.*1501C>A	ENSP00000501648.1:n.*1501C>A
ENST00000347559.6:c.1656C>A	ENSP00000292304.3:p.Arg552=
ENST00000368299.7:c.1746C>A	ENSP00000357282.3:p.Arg582=
ENST00000368300.8:c.1746C>A	ENSP00000357283.4:p.Arg582=
ENST00000448611.6:c.1410C>A	ENSP00000395597.2:p.Arg470=
ENST00000473598.6:c.1449C>A	ENSP00000421821.1:p.Arg483=
ENST00000496738.5:n.1959C>A
ENST00000506981.1:n.330C>A
ENST00000508500.1:c.534C>A	ENSP00000424977.1:p.Arg178=
NM_001257374.2:c.1410C>A	NP_001244303.1:p.Arg470=
NM_001282626.1:c.1746C>A	NP_001269555.1:p.Arg582=
NM_170707.3:c.1746C>A	NP_733821.1:p.Arg582=
NM_170708.3:c.1656C>A	NP_733822.1:p.Arg552=
XM_011509533.1:c.1410C>A	XP_011507835.1:p.Arg470=
XM_011509534.1:c.1122C>A	XP_011507836.1:p.Arg374=
XR_921781.1:n.2035C>A
XM_011509534.2:c.1122C>A	XP_011507836.1:p.Arg374=
XR_921781.2:n.2033C>A
NM_170707.4:c.1746C>A MANE Select	NP_733821.1:p.Arg582=
NM_001257374.3:c.1410C>A	NP_001244303.1:p.Arg470=
NM_001282626.2:c.1746C>A	NP_001269555.1:p.Arg582=
NM_170708.4:c.1656C>A	NP_733822.1:p.Arg552=