Canonical Allele Identifier: CA421068768

Gene: LMNA

Linked Data

• MyVariant Identifiers: chr1:g.156105697A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156135906A>T , CM000663.2:g.156135906A>T	GRCh38
NC_000001.10:g.156105697A>T , CM000663.1:g.156105697A>T	GRCh37
NC_000001.9:g.154372321A>T	NCBI36
NG_008692.2:g.58334A>T , LRG_254:g.58334A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.384A>T	ENSP00000426535.3:p.Ala128=
ENST00000498722.3:n.174A>T
ENST00000682650.1:c.942A>T	ENSP00000506904.1:p.Ala314=
ENST00000683032.1:c.942A>T	ENSP00000506771.1:p.Ala314=
ENST00000684195.1:c.942A>T	ENSP00000508220.1:p.Ala314=
ENST00000361308.9:c.942A>T	ENSP00000355292.6:p.Ala314=
ENST00000368300.9:c.942A>T MANE Select	ENSP00000357283.4:p.Ala314=
ENST00000496738.6:n.1317A>T
ENST00000674518.1:c.*292A>T	ENSP00000502261.1:n.*292A>T
ENST00000674600.1:c.*741A>T	ENSP00000501666.1:n.*741A>T
ENST00000674720.1:c.942A>T	ENSP00000502798.1:p.Ala314=
ENST00000675431.1:n.635A>T
ENST00000675455.1:c.*742A>T	ENSP00000501795.1:n.*742A>T
ENST00000675667.1:c.942A>T	ENSP00000501803.1:p.Ala314=
ENST00000675874.1:c.*413A>T	ENSP00000501851.1:n.*413A>T
ENST00000675881.1:c.982A>T	ENSP00000501670.1:p.Ser328Cys
ENST00000675939.1:c.942A>T	ENSP00000502256.1:p.Ala314=
ENST00000675989.1:n.1317A>T
ENST00000676208.1:c.982A>T	ENSP00000502468.1:p.Ser328Cys
ENST00000676283.1:n.1317A>T
ENST00000676385.2:c.942A>T	ENSP00000502091.1:p.Ala314=
ENST00000676434.1:c.982A>T	ENSP00000501648.1:p.Ser328Cys
ENST00000677389.1:c.942A>T MANE Plus Clinical	ENSP00000503633.1:p.Ala314=
ENST00000347559.6:c.942A>T	ENSP00000292304.3:p.Ala314=
ENST00000361308.8:c.942A>T	ENSP00000355292.5:p.Ala314=
ENST00000368297.5:c.699A>T	ENSP00000357280.1:p.Ala233=
ENST00000368298.2:n.206A>T
ENST00000368299.7:c.942A>T	ENSP00000357282.3:p.Ala314=
ENST00000368300.8:c.942A>T	ENSP00000357283.4:p.Ala314=
ENST00000368301.6:c.942A>T	ENSP00000357284.2:p.Ala314=
ENST00000448611.6:c.606A>T	ENSP00000395597.2:p.Ala202=
ENST00000473598.6:c.645A>T	ENSP00000421821.1:p.Ala215=
ENST00000496738.5:n.327A>T
ENST00000498722.2:n.174A>T
NM_001257374.2:c.606A>T	NP_001244303.1:p.Ala202=
NM_001282624.1:c.699A>T	NP_001269553.1:p.Ala233=
NM_001282625.1:c.942A>T	NP_001269554.1:p.Ala314=
NM_001282626.1:c.942A>T	NP_001269555.1:p.Ala314=
NM_005572.3:c.942A>T , LRG_254t1:c.942A>T	NP_005563.1:p.Ala314=
NM_170707.3:c.942A>T	NP_733821.1:p.Ala314=
NM_170708.3:c.942A>T	NP_733822.1:p.Ala314=
XM_011509533.1:c.606A>T	XP_011507835.1:p.Ala202=
XM_011509534.1:c.318A>T	XP_011507836.1:p.Ala106=
XR_921781.1:n.1231A>T
XM_011509534.2:c.318A>T	XP_011507836.1:p.Ala106=
XR_921781.2:n.1229A>T
NM_170707.4:c.942A>T MANE Select	NP_733821.1:p.Ala314=
NM_001257374.3:c.606A>T	NP_001244303.1:p.Ala202=
NM_001282626.2:c.942A>T	NP_001269555.1:p.Ala314=
NM_001282624.2:c.699A>T	NP_001269553.1:p.Ala233=
NM_001282625.2:c.942A>T	NP_001269554.1:p.Ala314=
NM_005572.4:c.942A>T MANE Plus Clinical	NP_005563.1:p.Ala314=
NM_170708.4:c.942A>T	NP_733822.1:p.Ala314=