Canonical Allele Identifier: CA342820040

Gene: LMNA

Linked Data

• MyVariant Identifiers: chr1:g.156105726A>C (hg19) ; chr1:g.156135935A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156135935A>C , CM000663.2:g.156135935A>C	GRCh38
NC_000001.10:g.156105726A>C , CM000663.1:g.156105726A>C	GRCh37
NC_000001.9:g.154372350A>C	NCBI36
NG_008692.2:g.58363A>C , LRG_254:g.58363A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000504687.7:c.413A>C	ENSP00000426535.3:p.Glu138Ala
ENST00000498722.3:n.203A>C
ENST00000682650.1:c.971A>C	ENSP00000506904.1:p.Glu324Ala
ENST00000683032.1:c.971A>C	ENSP00000506771.1:p.Glu324Ala
ENST00000684195.1:c.971A>C	ENSP00000508220.1:p.Glu324Ala
ENST00000361308.9:c.971A>C	ENSP00000355292.6:p.Glu324Ala
ENST00000368300.9:c.971A>C MANE Select	ENSP00000357283.4:p.Glu324Ala
ENST00000496738.6:n.1346A>C
ENST00000674518.1:c.*321A>C	ENSP00000502261.1:n.*321A>C
ENST00000674600.1:c.*770A>C	ENSP00000501666.1:n.*770A>C
ENST00000674720.1:c.971A>C	ENSP00000502798.1:p.Glu324Ala
ENST00000675431.1:n.664A>C
ENST00000675455.1:c.*771A>C	ENSP00000501795.1:n.*771A>C
ENST00000675667.1:c.971A>C	ENSP00000501803.1:p.Glu324Ala
ENST00000675874.1:c.*442A>C	ENSP00000501851.1:n.*442A>C
ENST00000675881.1:c.1011A>C	ENSP00000501670.1:p.Gly337=
ENST00000675939.1:c.971A>C	ENSP00000502256.1:p.Glu324Ala
ENST00000675989.1:n.1346A>C
ENST00000676208.1:c.1011A>C	ENSP00000502468.1:p.Gly337=
ENST00000676283.1:n.1346A>C
ENST00000676385.2:c.971A>C	ENSP00000502091.1:p.Glu324Ala
ENST00000676434.1:c.1011A>C	ENSP00000501648.1:p.Gly337=
ENST00000677389.1:c.971A>C MANE Plus Clinical	ENSP00000503633.1:p.Glu324Ala
ENST00000347559.6:c.971A>C	ENSP00000292304.3:p.Glu324Ala
ENST00000361308.8:c.971A>C	ENSP00000355292.5:p.Glu324Ala
ENST00000368297.5:c.728A>C	ENSP00000357280.1:p.Glu243Ala
ENST00000368298.2:n.235A>C
ENST00000368299.7:c.971A>C	ENSP00000357282.3:p.Glu324Ala
ENST00000368300.8:c.971A>C	ENSP00000357283.4:p.Glu324Ala
ENST00000368301.6:c.971A>C	ENSP00000357284.2:p.Glu324Ala
ENST00000448611.6:c.635A>C	ENSP00000395597.2:p.Glu212Ala
ENST00000473598.6:c.674A>C	ENSP00000421821.1:p.Glu225Ala
ENST00000496738.5:n.356A>C
ENST00000498722.2:n.203A>C
NM_001257374.2:c.635A>C	NP_001244303.1:p.Glu212Ala
NM_001282624.1:c.728A>C	NP_001269553.1:p.Glu243Ala
NM_001282625.1:c.971A>C	NP_001269554.1:p.Glu324Ala
NM_001282626.1:c.971A>C	NP_001269555.1:p.Glu324Ala
NM_005572.3:c.971A>C , LRG_254t1:c.971A>C	NP_005563.1:p.Glu324Ala
NM_170707.3:c.971A>C	NP_733821.1:p.Glu324Ala
NM_170708.3:c.971A>C	NP_733822.1:p.Glu324Ala
XM_011509533.1:c.635A>C	XP_011507835.1:p.Glu212Ala
XM_011509534.1:c.347A>C	XP_011507836.1:p.Glu116Ala
XR_921781.1:n.1260A>C
XM_011509534.2:c.347A>C	XP_011507836.1:p.Glu116Ala
XR_921781.2:n.1258A>C
NM_170707.4:c.971A>C MANE Select	NP_733821.1:p.Glu324Ala
NM_001257374.3:c.635A>C	NP_001244303.1:p.Glu212Ala
NM_001282626.2:c.971A>C	NP_001269555.1:p.Glu324Ala
NM_001282624.2:c.728A>C	NP_001269553.1:p.Glu243Ala
NM_001282625.2:c.971A>C	NP_001269554.1:p.Glu324Ala
NM_005572.4:c.971A>C MANE Plus Clinical	NP_005563.1:p.Glu324Ala
NM_170708.4:c.971A>C	NP_733822.1:p.Glu324Ala