Canonical Allele Identifier: CA421257990

Gene: LMNA

Linked Data

• MyVariant Identifiers: chr1:g.156106065A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156136274A>T , CM000663.2:g.156136274A>T	GRCh38
NC_000001.10:g.156106065A>T , CM000663.1:g.156106065A>T	GRCh37
NC_000001.9:g.154372689A>T	NCBI36
NG_008692.2:g.58702A>T , LRG_254:g.58702A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000504687.7:c.660A>T	ENSP00000426535.3:p.Ser220=
ENST00000498722.3:n.450A>T
ENST00000682650.1:c.1218A>T	ENSP00000506904.1:p.Ser406=
ENST00000683032.1:c.1218A>T	ENSP00000506771.1:p.Ser406=
ENST00000684195.1:c.1218A>T	ENSP00000508220.1:p.Ser406=
ENST00000361308.9:c.1218A>T	ENSP00000355292.6:p.Ser406=
ENST00000368300.9:c.1218A>T MANE Select	ENSP00000357283.4:p.Ser406=
ENST00000496738.6:n.1593A>T
ENST00000674518.1:c.*568A>T	ENSP00000502261.1:n.*568A>T
ENST00000674600.1:c.*1017A>T	ENSP00000501666.1:n.*1017A>T
ENST00000674720.1:c.1218A>T	ENSP00000502798.1:p.Ser406=
ENST00000675431.1:n.911A>T
ENST00000675455.1:c.*1018A>T	ENSP00000501795.1:n.*1018A>T
ENST00000675667.1:c.1218A>T	ENSP00000501803.1:p.Ser406=
ENST00000675874.1:c.*689A>T	ENSP00000501851.1:n.*689A>T
ENST00000675881.1:c.*229A>T	ENSP00000501670.1:n.*229A>T
ENST00000675939.1:c.1218A>T	ENSP00000502256.1:p.Ser406=
ENST00000675989.1:n.1593A>T
ENST00000676208.1:c.*321A>T	ENSP00000502468.1:n.*321A>T
ENST00000676283.1:n.1593A>T
ENST00000676385.2:c.1218A>T	ENSP00000502091.1:p.Ser406=
ENST00000676434.1:c.*229A>T	ENSP00000501648.1:n.*229A>T
ENST00000677389.1:c.1218A>T MANE Plus Clinical	ENSP00000503633.1:p.Ser406=
ENST00000347559.6:c.1218A>T	ENSP00000292304.3:p.Ser406=
ENST00000361308.8:c.1218A>T	ENSP00000355292.5:p.Ser406=
ENST00000368297.5:c.975A>T	ENSP00000357280.1:p.Ser325=
ENST00000368298.2:n.482A>T
ENST00000368299.7:c.1218A>T	ENSP00000357282.3:p.Ser406=
ENST00000368300.8:c.1218A>T	ENSP00000357283.4:p.Ser406=
ENST00000368301.6:c.1218A>T	ENSP00000357284.2:p.Ser406=
ENST00000448611.6:c.882A>T	ENSP00000395597.2:p.Ser294=
ENST00000473598.6:c.921A>T	ENSP00000421821.1:p.Ser307=
ENST00000496738.5:n.603A>T
ENST00000498722.2:n.450A>T
ENST00000508500.1:c.96A>T	ENSP00000424977.1:p.Ser32=
NM_001257374.2:c.882A>T	NP_001244303.1:p.Ser294=
NM_001282624.1:c.975A>T	NP_001269553.1:p.Ser325=
NM_001282625.1:c.1218A>T	NP_001269554.1:p.Ser406=
NM_001282626.1:c.1218A>T	NP_001269555.1:p.Ser406=
NM_005572.3:c.1218A>T , LRG_254t1:c.1218A>T	NP_005563.1:p.Ser406=
NM_170707.3:c.1218A>T	NP_733821.1:p.Ser406=
NM_170708.3:c.1218A>T	NP_733822.1:p.Ser406=
XM_011509533.1:c.882A>T	XP_011507835.1:p.Ser294=
XM_011509534.1:c.594A>T	XP_011507836.1:p.Ser198=
XR_921781.1:n.1507A>T
XM_011509534.2:c.594A>T	XP_011507836.1:p.Ser198=
XR_921781.2:n.1505A>T
NM_170707.4:c.1218A>T MANE Select	NP_733821.1:p.Ser406=
NM_001257374.3:c.882A>T	NP_001244303.1:p.Ser294=
NM_001282626.2:c.1218A>T	NP_001269555.1:p.Ser406=
NM_001282624.2:c.975A>T	NP_001269553.1:p.Ser325=
NM_001282625.2:c.1218A>T	NP_001269554.1:p.Ser406=
NM_005572.4:c.1218A>T MANE Plus Clinical	NP_005563.1:p.Ser406=
NM_170708.4:c.1218A>T	NP_733822.1:p.Ser406=