Canonical Allele Identifier: CA342819989

Gene: LMNA

Linked Data

• ClinVar Variation Id: 993352
• ClinVar RCV Id: RCV001812288
• dbSNP Id: rs1651541047
• MyVariant Identifiers: chr1:g.156105719G>A (hg19) ; chr1:g.156135928G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156135928G>A , CM000663.2:g.156135928G>A	GRCh38
NC_000001.10:g.156105719G>A , CM000663.1:g.156105719G>A	GRCh37
NC_000001.9:g.154372343G>A	NCBI36
NG_008692.2:g.58356G>A , LRG_254:g.58356G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000504687.7:c.406G>A	ENSP00000426535.3:p.Asp136Asn
ENST00000498722.3:n.196G>A
ENST00000682650.1:c.964G>A	ENSP00000506904.1:p.Asp322Asn
ENST00000683032.1:c.964G>A	ENSP00000506771.1:p.Asp322Asn
ENST00000684195.1:c.964G>A	ENSP00000508220.1:p.Asp322Asn
ENST00000361308.9:c.964G>A	ENSP00000355292.6:p.Asp322Asn
ENST00000368300.9:c.964G>A MANE Select	ENSP00000357283.4:p.Asp322Asn
ENST00000496738.6:n.1339G>A
ENST00000674518.1:c.*314G>A	ENSP00000502261.1:n.*314G>A
ENST00000674600.1:c.*763G>A	ENSP00000501666.1:n.*763G>A
ENST00000674720.1:c.964G>A	ENSP00000502798.1:p.Asp322Asn
ENST00000675431.1:n.657G>A
ENST00000675455.1:c.*764G>A	ENSP00000501795.1:n.*764G>A
ENST00000675667.1:c.964G>A	ENSP00000501803.1:p.Asp322Asn
ENST00000675874.1:c.*435G>A	ENSP00000501851.1:n.*435G>A
ENST00000675881.1:c.1004G>A	ENSP00000501670.1:p.Arg335Lys
ENST00000675939.1:c.964G>A	ENSP00000502256.1:p.Asp322Asn
ENST00000675989.1:n.1339G>A
ENST00000676208.1:c.1004G>A	ENSP00000502468.1:p.Arg335Lys
ENST00000676283.1:n.1339G>A
ENST00000676385.2:c.964G>A	ENSP00000502091.1:p.Asp322Asn
ENST00000676434.1:c.1004G>A	ENSP00000501648.1:p.Arg335Lys
ENST00000677389.1:c.964G>A MANE Plus Clinical	ENSP00000503633.1:p.Asp322Asn
ENST00000347559.6:c.964G>A	ENSP00000292304.3:p.Asp322Asn
ENST00000361308.8:c.964G>A	ENSP00000355292.5:p.Asp322Asn
ENST00000368297.5:c.721G>A	ENSP00000357280.1:p.Asp241Asn
ENST00000368298.2:n.228G>A
ENST00000368299.7:c.964G>A	ENSP00000357282.3:p.Asp322Asn
ENST00000368300.8:c.964G>A	ENSP00000357283.4:p.Asp322Asn
ENST00000368301.6:c.964G>A	ENSP00000357284.2:p.Asp322Asn
ENST00000448611.6:c.628G>A	ENSP00000395597.2:p.Asp210Asn
ENST00000473598.6:c.667G>A	ENSP00000421821.1:p.Asp223Asn
ENST00000496738.5:n.349G>A
ENST00000498722.2:n.196G>A
NM_001257374.2:c.628G>A	NP_001244303.1:p.Asp210Asn
NM_001282624.1:c.721G>A	NP_001269553.1:p.Asp241Asn
NM_001282625.1:c.964G>A	NP_001269554.1:p.Asp322Asn
NM_001282626.1:c.964G>A	NP_001269555.1:p.Asp322Asn
NM_005572.3:c.964G>A , LRG_254t1:c.964G>A	NP_005563.1:p.Asp322Asn
NM_170707.3:c.964G>A	NP_733821.1:p.Asp322Asn
NM_170708.3:c.964G>A	NP_733822.1:p.Asp322Asn
XM_011509533.1:c.628G>A	XP_011507835.1:p.Asp210Asn
XM_011509534.1:c.340G>A	XP_011507836.1:p.Asp114Asn
XR_921781.1:n.1253G>A
XM_011509534.2:c.340G>A	XP_011507836.1:p.Asp114Asn
XR_921781.2:n.1251G>A
NM_170707.4:c.964G>A MANE Select	NP_733821.1:p.Asp322Asn
NM_001257374.3:c.628G>A	NP_001244303.1:p.Asp210Asn
NM_001282626.2:c.964G>A	NP_001269555.1:p.Asp322Asn
NM_001282624.2:c.721G>A	NP_001269553.1:p.Asp241Asn
NM_001282625.2:c.964G>A	NP_001269554.1:p.Asp322Asn
NM_005572.4:c.964G>A MANE Plus Clinical	NP_005563.1:p.Asp322Asn
NM_170708.4:c.964G>A	NP_733822.1:p.Asp322Asn