Canonical Allele Identifier: CA10584126

Gene: LMNA

Linked Data

• ClinVar Variation Id: 246226
• ClinVar RCV Id: RCV000235905 ; RCV001038975 ; RCV001256917
• dbSNP Id: rs879254162
• gnomAD v4: 1-156136087-G-A
• COSMIC: COSM4698225 ; COSM4698226
• MyVariant Identifiers: chr1:g.156105878G>A (hg19) ; chr1:g.156136087G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156136087G>A , CM000663.2:g.156136087G>A	GRCh38
NC_000001.10:g.156105878G>A , CM000663.1:g.156105878G>A	GRCh37
NC_000001.9:g.154372502G>A	NCBI36
NG_008692.2:g.58515G>A , LRG_254:g.58515G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.565G>A	ENSP00000426535.3:p.Ala189Thr
ENST00000498722.3:n.355G>A
ENST00000682650.1:c.1123G>A	ENSP00000506904.1:p.Ala375Thr
ENST00000683032.1:c.1123G>A	ENSP00000506771.1:p.Ala375Thr
ENST00000684195.1:c.1123G>A	ENSP00000508220.1:p.Ala375Thr
ENST00000361308.9:c.1123G>A	ENSP00000355292.6:p.Ala375Thr
ENST00000368300.9:c.1123G>A MANE Select	ENSP00000357283.4:p.Ala375Thr
ENST00000496738.6:n.1498G>A
ENST00000674518.1:c.*473G>A	ENSP00000502261.1:n.*473G>A
ENST00000674600.1:c.*922G>A	ENSP00000501666.1:n.*922G>A
ENST00000674720.1:c.1123G>A	ENSP00000502798.1:p.Ala375Thr
ENST00000675431.1:n.816G>A
ENST00000675455.1:c.*923G>A	ENSP00000501795.1:n.*923G>A
ENST00000675667.1:c.1123G>A	ENSP00000501803.1:p.Ala375Thr
ENST00000675874.1:c.*594G>A	ENSP00000501851.1:n.*594G>A
ENST00000675881.1:c.*134G>A	ENSP00000501670.1:n.*134G>A
ENST00000675939.1:c.1123G>A	ENSP00000502256.1:p.Ala375Thr
ENST00000675989.1:n.1498G>A
ENST00000676208.1:c.*134G>A	ENSP00000502468.1:n.*134G>A
ENST00000676283.1:n.1498G>A
ENST00000676385.2:c.1123G>A	ENSP00000502091.1:p.Ala375Thr
ENST00000676434.1:c.*134G>A	ENSP00000501648.1:n.*134G>A
ENST00000677389.1:c.1123G>A MANE Plus Clinical	ENSP00000503633.1:p.Ala375Thr
ENST00000347559.6:c.1123G>A	ENSP00000292304.3:p.Ala375Thr
ENST00000361308.8:c.1123G>A	ENSP00000355292.5:p.Ala375Thr
ENST00000368297.5:c.880G>A	ENSP00000357280.1:p.Ala294Thr
ENST00000368298.2:n.387G>A
ENST00000368299.7:c.1123G>A	ENSP00000357282.3:p.Ala375Thr
ENST00000368300.8:c.1123G>A	ENSP00000357283.4:p.Ala375Thr
ENST00000368301.6:c.1123G>A	ENSP00000357284.2:p.Ala375Thr
ENST00000448611.6:c.787G>A	ENSP00000395597.2:p.Ala263Thr
ENST00000473598.6:c.826G>A	ENSP00000421821.1:p.Ala276Thr
ENST00000496738.5:n.508G>A
ENST00000498722.2:n.355G>A
ENST00000508500.1:c.1G>A	ENSP00000424977.1:p.Ala1Thr
NM_001257374.2:c.787G>A	NP_001244303.1:p.Ala263Thr
NM_001282624.1:c.880G>A	NP_001269553.1:p.Ala294Thr
NM_001282625.1:c.1123G>A	NP_001269554.1:p.Ala375Thr
NM_001282626.1:c.1123G>A	NP_001269555.1:p.Ala375Thr
NM_005572.3:c.1123G>A , LRG_254t1:c.1123G>A	NP_005563.1:p.Ala375Thr
NM_170707.3:c.1123G>A	NP_733821.1:p.Ala375Thr
NM_170708.3:c.1123G>A	NP_733822.1:p.Ala375Thr
XM_011509533.1:c.787G>A	XP_011507835.1:p.Ala263Thr
XM_011509534.1:c.499G>A	XP_011507836.1:p.Ala167Thr
XR_921781.1:n.1412G>A
XM_011509534.2:c.499G>A	XP_011507836.1:p.Ala167Thr
XR_921781.2:n.1410G>A
NM_170707.4:c.1123G>A MANE Select	NP_733821.1:p.Ala375Thr
NM_001257374.3:c.787G>A	NP_001244303.1:p.Ala263Thr
NM_001282626.2:c.1123G>A	NP_001269555.1:p.Ala375Thr
NM_001282624.2:c.880G>A	NP_001269553.1:p.Ala294Thr
NM_001282625.2:c.1123G>A	NP_001269554.1:p.Ala375Thr
NM_005572.4:c.1123G>A MANE Plus Clinical	NP_005563.1:p.Ala375Thr
NM_170708.4:c.1123G>A	NP_733822.1:p.Ala375Thr