Canonical Allele Identifier: CA16609888

Gene: LMNA

Linked Data

• ClinVar Variation Id: 408993
• ClinVar RCV Id: RCV000458536
• dbSNP Id: rs1060502214
• MyVariant Identifiers: chr1:g.156105873T>G (hg19) ; chr1:g.156136082T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156136082T>G , CM000663.2:g.156136082T>G	GRCh38
NC_000001.10:g.156105873T>G , CM000663.1:g.156105873T>G	GRCh37
NC_000001.9:g.154372497T>G	NCBI36
NG_008692.2:g.58510T>G , LRG_254:g.58510T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.560T>G	ENSP00000426535.3:p.Ile187Ser
ENST00000498722.3:n.350T>G
ENST00000682650.1:c.1118T>G	ENSP00000506904.1:p.Ile373Ser
ENST00000683032.1:c.1118T>G	ENSP00000506771.1:p.Ile373Ser
ENST00000684195.1:c.1118T>G	ENSP00000508220.1:p.Ile373Ser
ENST00000361308.9:c.1118T>G	ENSP00000355292.6:p.Ile373Ser
ENST00000368300.9:c.1118T>G MANE Select	ENSP00000357283.4:p.Ile373Ser
ENST00000496738.6:n.1493T>G
ENST00000674518.1:c.*468T>G	ENSP00000502261.1:n.*468T>G
ENST00000674600.1:c.*917T>G	ENSP00000501666.1:n.*917T>G
ENST00000674720.1:c.1118T>G	ENSP00000502798.1:p.Ile373Ser
ENST00000675431.1:n.811T>G
ENST00000675455.1:c.*918T>G	ENSP00000501795.1:n.*918T>G
ENST00000675667.1:c.1118T>G	ENSP00000501803.1:p.Ile373Ser
ENST00000675874.1:c.*589T>G	ENSP00000501851.1:n.*589T>G
ENST00000675881.1:c.*129T>G	ENSP00000501670.1:n.*129T>G
ENST00000675939.1:c.1118T>G	ENSP00000502256.1:p.Ile373Ser
ENST00000675989.1:n.1493T>G
ENST00000676208.1:c.*129T>G	ENSP00000502468.1:n.*129T>G
ENST00000676283.1:n.1493T>G
ENST00000676385.2:c.1118T>G	ENSP00000502091.1:p.Ile373Ser
ENST00000676434.1:c.*129T>G	ENSP00000501648.1:n.*129T>G
ENST00000677389.1:c.1118T>G MANE Plus Clinical	ENSP00000503633.1:p.Ile373Ser
ENST00000347559.6:c.1118T>G	ENSP00000292304.3:p.Ile373Ser
ENST00000361308.8:c.1118T>G	ENSP00000355292.5:p.Ile373Ser
ENST00000368297.5:c.875T>G	ENSP00000357280.1:p.Ile292Ser
ENST00000368298.2:n.382T>G
ENST00000368299.7:c.1118T>G	ENSP00000357282.3:p.Ile373Ser
ENST00000368300.8:c.1118T>G	ENSP00000357283.4:p.Ile373Ser
ENST00000368301.6:c.1118T>G	ENSP00000357284.2:p.Ile373Ser
ENST00000448611.6:c.782T>G	ENSP00000395597.2:p.Ile261Ser
ENST00000473598.6:c.821T>G	ENSP00000421821.1:p.Ile274Ser
ENST00000496738.5:n.503T>G
ENST00000498722.2:n.350T>G
NM_001257374.2:c.782T>G	NP_001244303.1:p.Ile261Ser
NM_001282624.1:c.875T>G	NP_001269553.1:p.Ile292Ser
NM_001282625.1:c.1118T>G	NP_001269554.1:p.Ile373Ser
NM_001282626.1:c.1118T>G	NP_001269555.1:p.Ile373Ser
NM_005572.3:c.1118T>G , LRG_254t1:c.1118T>G	NP_005563.1:p.Ile373Ser
NM_170707.3:c.1118T>G	NP_733821.1:p.Ile373Ser
NM_170708.3:c.1118T>G	NP_733822.1:p.Ile373Ser
XM_011509533.1:c.782T>G	XP_011507835.1:p.Ile261Ser
XM_011509534.1:c.494T>G	XP_011507836.1:p.Ile165Ser
XR_921781.1:n.1407T>G
XM_011509534.2:c.494T>G	XP_011507836.1:p.Ile165Ser
XR_921781.2:n.1405T>G
NM_170707.4:c.1118T>G MANE Select	NP_733821.1:p.Ile373Ser
NM_001257374.3:c.782T>G	NP_001244303.1:p.Ile261Ser
NM_001282626.2:c.1118T>G	NP_001269555.1:p.Ile373Ser
NM_001282624.2:c.875T>G	NP_001269553.1:p.Ile292Ser
NM_001282625.2:c.1118T>G	NP_001269554.1:p.Ile373Ser
NM_005572.4:c.1118T>G MANE Plus Clinical	NP_005563.1:p.Ile373Ser
NM_170708.4:c.1118T>G	NP_733822.1:p.Ile373Ser