Canonical Allele Identifier: CA421257577

Gene: LMNA

Linked Data

• ClinVar Variation Id: 1382049
• ClinVar RCV Id: RCV001897371 ; RCV002343962 ; RCV004010754
• dbSNP Id: rs1437725392
• gnomAD v2: 1-156104220-G-A
• gnomAD v3: 1-156134429-G-A
• gnomAD v4: 1-156134429-G-A
• MyVariant Identifiers: chr1:g.156104220G>A (hg19) ; chr1:g.156134429G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156134429G>A , CM000663.2:g.156134429G>A	GRCh38
NC_000001.10:g.156104220G>A , CM000663.1:g.156104220G>A	GRCh37
NC_000001.9:g.154370844G>A	NCBI36
NG_008692.2:g.56857G>A , LRG_254:g.56857G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.-19G>A	ENSP00000426535.3:n.-19G>A
ENST00000682650.1:c.540G>A	ENSP00000506904.1:p.Lys180=
ENST00000683032.1:c.540G>A	ENSP00000506771.1:p.Lys180=
ENST00000684195.1:c.540G>A	ENSP00000508220.1:p.Lys180=
ENST00000361308.9:c.540G>A	ENSP00000355292.6:p.Lys180=
ENST00000368300.9:c.540G>A MANE Select	ENSP00000357283.4:p.Lys180=
ENST00000496738.6:n.915G>A
ENST00000504687.6:c.-125G>A	ENSP00000426535.2:n.-125G>A
ENST00000674518.1:c.540G>A	ENSP00000502261.1:p.Lys180=
ENST00000674600.1:c.*339G>A	ENSP00000501666.1:n.*339G>A
ENST00000674720.1:c.540G>A	ENSP00000502798.1:p.Lys180=
ENST00000675431.1:n.233G>A
ENST00000675455.1:c.*340G>A	ENSP00000501795.1:n.*340G>A
ENST00000675667.1:c.540G>A	ENSP00000501803.1:p.Lys180=
ENST00000675874.1:c.*11G>A	ENSP00000501851.1:n.*11G>A
ENST00000675881.1:c.540G>A	ENSP00000501670.1:p.Lys180=
ENST00000675939.1:c.540G>A	ENSP00000502256.1:p.Lys180=
ENST00000675989.1:n.915G>A
ENST00000676208.1:c.540G>A	ENSP00000502468.1:p.Lys180=
ENST00000676283.1:n.915G>A
ENST00000676385.2:c.540G>A	ENSP00000502091.1:p.Lys180=
ENST00000676434.1:c.540G>A	ENSP00000501648.1:p.Lys180=
ENST00000677389.1:c.540G>A MANE Plus Clinical	ENSP00000503633.1:p.Lys180=
ENST00000347559.6:c.540G>A	ENSP00000292304.3:p.Lys180=
ENST00000361308.8:c.540G>A	ENSP00000355292.5:p.Lys180=
ENST00000368297.5:c.297G>A	ENSP00000357280.1:p.Lys99=
ENST00000368299.7:c.540G>A	ENSP00000357282.3:p.Lys180=
ENST00000368300.8:c.540G>A	ENSP00000357283.4:p.Lys180=
ENST00000368301.6:c.540G>A	ENSP00000357284.2:p.Lys180=
ENST00000448611.6:c.204G>A	ENSP00000395597.2:p.Lys68=
ENST00000469565.6:n.574G>A
ENST00000470199.2:n.482G>A
ENST00000473598.6:c.243G>A	ENSP00000421821.1:p.Lys81=
ENST00000502357.5:n.438G>A
ENST00000502751.5:n.512G>A
ENST00000504687.5:c.291G>A	ENSP00000426535.1:p.Lys97=
ENST00000515459.5:c.*214G>A	ENSP00000424518.1:n.*214G>A
NM_001257374.2:c.204G>A	NP_001244303.1:p.Lys68=
NM_001282624.1:c.297G>A	NP_001269553.1:p.Lys99=
NM_001282625.1:c.540G>A	NP_001269554.1:p.Lys180=
NM_001282626.1:c.540G>A	NP_001269555.1:p.Lys180=
NM_005572.3:c.540G>A , LRG_254t1:c.540G>A	NP_005563.1:p.Lys180=
NM_170707.3:c.540G>A	NP_733821.1:p.Lys180=
NM_170708.3:c.540G>A	NP_733822.1:p.Lys180=
XM_011509533.1:c.204G>A	XP_011507835.1:p.Lys68=
XM_011509534.1:c.-125G>A	XP_011507836.1:n.-125G>A
XR_921781.1:n.789G>A
XM_011509534.2:c.-125G>A	XP_011507836.1:n.-125G>A
XR_921781.2:n.787G>A
NM_170707.4:c.540G>A MANE Select	NP_733821.1:p.Lys180=
NM_001257374.3:c.204G>A	NP_001244303.1:p.Lys68=
NM_001282626.2:c.540G>A	NP_001269555.1:p.Lys180=
NM_001282624.2:c.297G>A	NP_001269553.1:p.Lys99=
NM_001282625.2:c.540G>A	NP_001269554.1:p.Lys180=
NM_005572.4:c.540G>A MANE Plus Clinical	NP_005563.1:p.Lys180=
NM_170708.4:c.540G>A	NP_733822.1:p.Lys180=