Canonical Allele Identifier: CA421257933

Gene: LMNA

Linked Data

• MyVariant Identifiers: chr1:g.156108350C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156138559C>A , CM000663.2:g.156138559C>A	GRCh38
NC_000001.10:g.156108350C>A , CM000663.1:g.156108350C>A	GRCh37
NC_000001.9:g.154374974C>A	NCBI36
NG_008692.2:g.60987C>A , LRG_254:g.60987C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.1212C>A	ENSP00000426535.3:p.Thr404=
ENST00000682650.1:c.1680C>A	ENSP00000506904.1:p.Thr560=
ENST00000683032.1:c.1770C>A	ENSP00000506771.1:p.Thr590=
ENST00000683773.1:n.115C>A
ENST00000684195.1:c.*862C>A	ENSP00000508220.1:n.*862C>A
ENST00000361308.9:c.1770C>A	ENSP00000355292.6:p.Thr590=
ENST00000368300.9:c.1770C>A MANE Select	ENSP00000357283.4:p.Thr590=
ENST00000496738.6:n.2973C>A
ENST00000674518.1:c.*1120C>A	ENSP00000502261.1:n.*1120C>A
ENST00000674600.1:c.*1569C>A	ENSP00000501666.1:n.*1569C>A
ENST00000674720.1:c.*1076C>A	ENSP00000502798.1:n.*1076C>A
ENST00000675455.1:c.*1570C>A	ENSP00000501795.1:n.*1570C>A
ENST00000675667.1:c.1770C>A	ENSP00000501803.1:p.Thr590=
ENST00000675874.1:c.*1241C>A	ENSP00000501851.1:n.*1241C>A
ENST00000675881.1:c.*781C>A	ENSP00000501670.1:n.*781C>A
ENST00000675939.1:c.1770C>A	ENSP00000502256.1:p.Thr590=
ENST00000675989.1:n.3373C>A
ENST00000676208.1:c.*873C>A	ENSP00000502468.1:n.*873C>A
ENST00000676283.1:n.3310C>A
ENST00000676385.2:c.1680C>A	ENSP00000502091.1:p.Thr560=
ENST00000676434.1:c.*1525C>A	ENSP00000501648.1:n.*1525C>A
ENST00000347559.6:c.1680C>A	ENSP00000292304.3:p.Thr560=
ENST00000368299.7:c.1770C>A	ENSP00000357282.3:p.Thr590=
ENST00000368300.8:c.1770C>A	ENSP00000357283.4:p.Thr590=
ENST00000448611.6:c.1434C>A	ENSP00000395597.2:p.Thr478=
ENST00000473598.6:c.1473C>A	ENSP00000421821.1:p.Thr491=
ENST00000496738.5:n.1983C>A
ENST00000506981.1:n.354C>A
ENST00000508500.1:c.558C>A	ENSP00000424977.1:p.Thr186=
NM_001257374.2:c.1434C>A	NP_001244303.1:p.Thr478=
NM_001282626.1:c.1770C>A	NP_001269555.1:p.Thr590=
NM_170707.3:c.1770C>A	NP_733821.1:p.Thr590=
NM_170708.3:c.1680C>A	NP_733822.1:p.Thr560=
XM_011509533.1:c.1434C>A	XP_011507835.1:p.Thr478=
XM_011509534.1:c.1146C>A	XP_011507836.1:p.Thr382=
XR_921781.1:n.2059C>A
XM_011509534.2:c.1146C>A	XP_011507836.1:p.Thr382=
XR_921781.2:n.2057C>A
NM_170707.4:c.1770C>A MANE Select	NP_733821.1:p.Thr590=
NM_001257374.3:c.1434C>A	NP_001244303.1:p.Thr478=
NM_001282626.2:c.1770C>A	NP_001269555.1:p.Thr590=
NM_170708.4:c.1680C>A	NP_733822.1:p.Thr560=