Canonical Allele Identifier: CA342827495

Gene: LMNA

Linked Data

• dbSNP Id: rs398124550
• gnomAD v2: 1-156108453-A-G
• gnomAD v4: 1-156138662-A-G
• MyVariant Identifiers: chr1:g.156108453A>G (hg19) ; chr1:g.156138662A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156138662A>G , CM000663.2:g.156138662A>G	GRCh38
NC_000001.10:g.156108453A>G , CM000663.1:g.156108453A>G	GRCh37
NC_000001.9:g.154375077A>G	NCBI36
NG_008692.2:g.61090A>G , LRG_254:g.61090A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000504687.7:c.1315A>G	ENSP00000426535.3:p.Ser439Gly
ENST00000682650.1:c.1783A>G	ENSP00000506904.1:p.Ser595Gly
ENST00000683032.1:c.1873A>G	ENSP00000506771.1:p.Ser625Gly
ENST00000683773.1:n.163+55A>G
ENST00000684195.1:c.*965A>G	ENSP00000508220.1:n.*965A>G
ENST00000361308.9:c.1873A>G	ENSP00000355292.6:p.Ser625Gly
ENST00000368300.9:c.1873A>G MANE Select	ENSP00000357283.4:p.Ser625Gly
ENST00000674518.1:c.*1223A>G	ENSP00000502261.1:n.*1223A>G
ENST00000674600.1:c.*1672A>G	ENSP00000501666.1:n.*1672A>G
ENST00000675455.1:c.*1673A>G	ENSP00000501795.1:n.*1673A>G
ENST00000675667.1:c.1873A>G	ENSP00000501803.1:p.Ser625Gly
ENST00000675874.1:c.*1344A>G	ENSP00000501851.1:n.*1344A>G
ENST00000675881.1:c.*884A>G	ENSP00000501670.1:n.*884A>G
ENST00000675939.1:c.1873A>G	ENSP00000502256.1:p.Ser625Gly
ENST00000675989.1:n.3476A>G
ENST00000676208.1:c.*976A>G	ENSP00000502468.1:n.*976A>G
ENST00000676385.2:c.1783A>G	ENSP00000502091.1:p.Ser595Gly
ENST00000676434.1:c.*1628A>G	ENSP00000501648.1:n.*1628A>G
ENST00000347559.6:c.1783A>G	ENSP00000292304.3:p.Ser595Gly
ENST00000368299.7:c.1818+55A>G	ENSP00000357282.3:n.1818+55A>G
ENST00000368300.8:c.1873A>G	ENSP00000357283.4:p.Ser625Gly
ENST00000448611.6:c.1537A>G	ENSP00000395597.2:p.Ser513Gly
ENST00000473598.6:c.1576A>G	ENSP00000421821.1:p.Ser526Gly
ENST00000496738.5:n.2086A>G
ENST00000506981.1:n.457A>G
ENST00000508500.1:c.661A>G	ENSP00000424977.1:p.Ser221Gly
NM_001257374.2:c.1537A>G	NP_001244303.1:p.Ser513Gly
NM_001282626.1:c.1818+55A>G	NP_001269555.1:n.1818+55A>G
NM_170707.3:c.1873A>G	NP_733821.1:p.Ser625Gly
NM_170708.3:c.1783A>G	NP_733822.1:p.Ser595Gly
XM_011509533.1:c.1537A>G	XP_011507835.1:p.Ser513Gly
XM_011509534.1:c.1249A>G	XP_011507836.1:p.Ser417Gly
XR_921781.1:n.2162A>G
XM_011509534.2:c.1249A>G	XP_011507836.1:p.Ser417Gly
XR_921781.2:n.2160A>G
NM_170707.4:c.1873A>G MANE Select	NP_733821.1:p.Ser625Gly
NM_001257374.3:c.1537A>G	NP_001244303.1:p.Ser513Gly
NM_001282626.2:c.1818+55A>G	NP_001269555.1:n.1818+55A>G
NM_170708.4:c.1783A>G	NP_733822.1:p.Ser595Gly