Canonical Allele Identifier: CA342823023

Gene: LMNA

Linked Data

• ClinVar Variation Id: 917431
• ClinVar RCV Id: RCV001174409
• dbSNP Id: rs1215424724
• gnomAD v2: 1-156106919-G-A
• gnomAD v3: 1-156137128-G-A
• gnomAD v4: 1-156137128-G-A
• MyVariant Identifiers: chr1:g.156106919G>A (hg19) ; chr1:g.156137128G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156137128G>A , CM000663.2:g.156137128G>A	GRCh38
NC_000001.10:g.156106919G>A , CM000663.1:g.156106919G>A	GRCh37
NC_000001.9:g.154373543G>A	NCBI36
NG_008692.2:g.59556G>A , LRG_254:g.59556G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000504687.7:c.946G>A	ENSP00000426535.3:p.Ala316Thr
ENST00000459904.2:n.752G>A
ENST00000498722.3:n.736G>A
ENST00000682650.1:c.1504G>A	ENSP00000506904.1:p.Ala502Thr
ENST00000683032.1:c.1504G>A	ENSP00000506771.1:p.Ala502Thr
ENST00000684195.1:c.1504G>A	ENSP00000508220.1:p.Ala502Thr
ENST00000361308.9:c.1504G>A	ENSP00000355292.6:p.Ala502Thr
ENST00000368300.9:c.1504G>A MANE Select	ENSP00000357283.4:p.Ala502Thr
ENST00000496738.6:n.1963G>A
ENST00000674518.1:c.*854G>A	ENSP00000502261.1:n.*854G>A
ENST00000674600.1:c.*1303G>A	ENSP00000501666.1:n.*1303G>A
ENST00000674720.1:c.*66G>A	ENSP00000502798.1:n.*66G>A
ENST00000675431.1:n.1197G>A
ENST00000675455.1:c.*1304G>A	ENSP00000501795.1:n.*1304G>A
ENST00000675667.1:c.1504G>A	ENSP00000501803.1:p.Ala502Thr
ENST00000675874.1:c.*975G>A	ENSP00000501851.1:n.*975G>A
ENST00000675881.1:c.*515G>A	ENSP00000501670.1:n.*515G>A
ENST00000675939.1:c.1504G>A	ENSP00000502256.1:p.Ala502Thr
ENST00000675989.1:n.2363G>A
ENST00000676208.1:c.*607G>A	ENSP00000502468.1:n.*607G>A
ENST00000676283.1:n.1879G>A
ENST00000676385.2:c.1504G>A	ENSP00000502091.1:p.Ala502Thr
ENST00000676434.1:c.*515G>A	ENSP00000501648.1:n.*515G>A
ENST00000677389.1:c.1504G>A MANE Plus Clinical	ENSP00000503633.1:p.Ala502Thr
ENST00000347559.6:c.1504G>A	ENSP00000292304.3:p.Ala502Thr
ENST00000361308.8:c.1312-63G>A	ENSP00000355292.5:n.1312-63G>A
ENST00000368297.5:c.1261G>A	ENSP00000357280.1:p.Ala421Thr
ENST00000368298.2:n.1336G>A
ENST00000368299.7:c.1504G>A	ENSP00000357282.3:p.Ala502Thr
ENST00000368300.8:c.1504G>A	ENSP00000357283.4:p.Ala502Thr
ENST00000368301.6:c.1504G>A	ENSP00000357284.2:p.Ala502Thr
ENST00000448611.6:c.1168G>A	ENSP00000395597.2:p.Ala390Thr
ENST00000459904.1:n.752G>A
ENST00000473598.6:c.1207G>A	ENSP00000421821.1:p.Ala403Thr
ENST00000496738.5:n.973G>A
ENST00000498722.2:n.736G>A
ENST00000508500.1:c.382G>A	ENSP00000424977.1:p.Ala128Thr
NM_001257374.2:c.1168G>A	NP_001244303.1:p.Ala390Thr
NM_001282624.1:c.1261G>A	NP_001269553.1:p.Ala421Thr
NM_001282625.1:c.1504G>A	NP_001269554.1:p.Ala502Thr
NM_001282626.1:c.1504G>A	NP_001269555.1:p.Ala502Thr
NM_005572.3:c.1504G>A , LRG_254t1:c.1504G>A	NP_005563.1:p.Ala502Thr
NM_170707.3:c.1504G>A	NP_733821.1:p.Ala502Thr
NM_170708.3:c.1504G>A	NP_733822.1:p.Ala502Thr
XM_011509533.1:c.1168G>A	XP_011507835.1:p.Ala390Thr
XM_011509534.1:c.880G>A	XP_011507836.1:p.Ala294Thr
XR_921781.1:n.1793G>A
XM_011509534.2:c.880G>A	XP_011507836.1:p.Ala294Thr
XR_921781.2:n.1791G>A
NM_170707.4:c.1504G>A MANE Select	NP_733821.1:p.Ala502Thr
NM_001257374.3:c.1168G>A	NP_001244303.1:p.Ala390Thr
NM_001282626.2:c.1504G>A	NP_001269555.1:p.Ala502Thr
NM_001282624.2:c.1261G>A	NP_001269553.1:p.Ala421Thr
NM_001282625.2:c.1504G>A	NP_001269554.1:p.Ala502Thr
NM_005572.4:c.1504G>A MANE Plus Clinical	NP_005563.1:p.Ala502Thr
NM_170708.4:c.1504G>A	NP_733822.1:p.Ala502Thr