Canonical Allele Identifier: CA421068771

Gene: LMNA

Linked Data

• ClinVar Variation Id: 1767029
• ClinVar RCV Id: RCV003094814 ; RCV002443477
• MyVariant Identifiers: chr1:g.156105700C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156135909C>T , CM000663.2:g.156135909C>T	GRCh38
NC_000001.10:g.156105700C>T , CM000663.1:g.156105700C>T	GRCh37
NC_000001.9:g.154372324C>T	NCBI36
NG_008692.2:g.58337C>T , LRG_254:g.58337C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.387C>T	ENSP00000426535.3:p.Ala129=
ENST00000498722.3:n.177C>T
ENST00000682650.1:c.945C>T	ENSP00000506904.1:p.Ala315=
ENST00000683032.1:c.945C>T	ENSP00000506771.1:p.Ala315=
ENST00000684195.1:c.945C>T	ENSP00000508220.1:p.Ala315=
ENST00000361308.9:c.945C>T	ENSP00000355292.6:p.Ala315=
ENST00000368300.9:c.945C>T MANE Select	ENSP00000357283.4:p.Ala315=
ENST00000496738.6:n.1320C>T
ENST00000674518.1:c.*295C>T	ENSP00000502261.1:n.*295C>T
ENST00000674600.1:c.*744C>T	ENSP00000501666.1:n.*744C>T
ENST00000674720.1:c.945C>T	ENSP00000502798.1:p.Ala315=
ENST00000675431.1:n.638C>T
ENST00000675455.1:c.*745C>T	ENSP00000501795.1:n.*745C>T
ENST00000675667.1:c.945C>T	ENSP00000501803.1:p.Ala315=
ENST00000675874.1:c.*416C>T	ENSP00000501851.1:n.*416C>T
ENST00000675881.1:c.985C>T	ENSP00000501670.1:p.Gln329Ter
ENST00000675939.1:c.945C>T	ENSP00000502256.1:p.Ala315=
ENST00000675989.1:n.1320C>T
ENST00000676208.1:c.985C>T	ENSP00000502468.1:p.Gln329Ter
ENST00000676283.1:n.1320C>T
ENST00000676385.2:c.945C>T	ENSP00000502091.1:p.Ala315=
ENST00000676434.1:c.985C>T	ENSP00000501648.1:p.Gln329Ter
ENST00000677389.1:c.945C>T MANE Plus Clinical	ENSP00000503633.1:p.Ala315=
ENST00000347559.6:c.945C>T	ENSP00000292304.3:p.Ala315=
ENST00000361308.8:c.945C>T	ENSP00000355292.5:p.Ala315=
ENST00000368297.5:c.702C>T	ENSP00000357280.1:p.Ala234=
ENST00000368298.2:n.209C>T
ENST00000368299.7:c.945C>T	ENSP00000357282.3:p.Ala315=
ENST00000368300.8:c.945C>T	ENSP00000357283.4:p.Ala315=
ENST00000368301.6:c.945C>T	ENSP00000357284.2:p.Ala315=
ENST00000448611.6:c.609C>T	ENSP00000395597.2:p.Ala203=
ENST00000473598.6:c.648C>T	ENSP00000421821.1:p.Ala216=
ENST00000496738.5:n.330C>T
ENST00000498722.2:n.177C>T
NM_001257374.2:c.609C>T	NP_001244303.1:p.Ala203=
NM_001282624.1:c.702C>T	NP_001269553.1:p.Ala234=
NM_001282625.1:c.945C>T	NP_001269554.1:p.Ala315=
NM_001282626.1:c.945C>T	NP_001269555.1:p.Ala315=
NM_005572.3:c.945C>T , LRG_254t1:c.945C>T	NP_005563.1:p.Ala315=
NM_170707.3:c.945C>T	NP_733821.1:p.Ala315=
NM_170708.3:c.945C>T	NP_733822.1:p.Ala315=
XM_011509533.1:c.609C>T	XP_011507835.1:p.Ala203=
XM_011509534.1:c.321C>T	XP_011507836.1:p.Ala107=
XR_921781.1:n.1234C>T
XM_011509534.2:c.321C>T	XP_011507836.1:p.Ala107=
XR_921781.2:n.1232C>T
NM_170707.4:c.945C>T MANE Select	NP_733821.1:p.Ala315=
NM_001257374.3:c.609C>T	NP_001244303.1:p.Ala203=
NM_001282626.2:c.945C>T	NP_001269555.1:p.Ala315=
NM_001282624.2:c.702C>T	NP_001269553.1:p.Ala234=
NM_001282625.2:c.945C>T	NP_001269554.1:p.Ala315=
NM_005572.4:c.945C>T MANE Plus Clinical	NP_005563.1:p.Ala315=
NM_170708.4:c.945C>T	NP_733822.1:p.Ala315=