Canonical Allele Identifier: CA16609891

Gene: LMNA

Linked Data

• ClinVar Variation Id: 408988
• ClinVar RCV Id: RCV000467141
• dbSNP Id: rs1060502211
• MyVariant Identifiers: chr1:g.156105743G>T (hg19) ; chr1:g.156135952G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156135952G>T , CM000663.2:g.156135952G>T	GRCh38
NC_000001.10:g.156105743G>T , CM000663.1:g.156105743G>T	GRCh37
NC_000001.9:g.154372367G>T	NCBI36
NG_008692.2:g.58380G>T , LRG_254:g.58380G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.430G>T	ENSP00000426535.3:p.Glu144Ter
ENST00000498722.3:n.220G>T
ENST00000682650.1:c.988G>T	ENSP00000506904.1:p.Glu330Ter
ENST00000683032.1:c.988G>T	ENSP00000506771.1:p.Glu330Ter
ENST00000684195.1:c.988G>T	ENSP00000508220.1:p.Glu330Ter
ENST00000361308.9:c.988G>T	ENSP00000355292.6:p.Glu330Ter
ENST00000368300.9:c.988G>T MANE Select	ENSP00000357283.4:p.Glu330Ter
ENST00000496738.6:n.1363G>T
ENST00000674518.1:c.*338G>T	ENSP00000502261.1:n.*338G>T
ENST00000674600.1:c.*787G>T	ENSP00000501666.1:n.*787G>T
ENST00000674720.1:c.988G>T	ENSP00000502798.1:p.Glu330Ter
ENST00000675431.1:n.681G>T
ENST00000675455.1:c.*788G>T	ENSP00000501795.1:n.*788G>T
ENST00000675667.1:c.988G>T	ENSP00000501803.1:p.Glu330Ter
ENST00000675874.1:c.*459G>T	ENSP00000501851.1:n.*459G>T
ENST00000675881.1:c.1028G>T	ENSP00000501670.1:p.Ter343Leu
ENST00000675939.1:c.988G>T	ENSP00000502256.1:p.Glu330Ter
ENST00000675989.1:n.1363G>T
ENST00000676208.1:c.1028G>T	ENSP00000502468.1:p.Ter343Leu
ENST00000676283.1:n.1363G>T
ENST00000676385.2:c.988G>T	ENSP00000502091.1:p.Glu330Ter
ENST00000676434.1:c.1028G>T	ENSP00000501648.1:p.Ter343Leu
ENST00000677389.1:c.988G>T MANE Plus Clinical	ENSP00000503633.1:p.Glu330Ter
ENST00000347559.6:c.988G>T	ENSP00000292304.3:p.Glu330Ter
ENST00000361308.8:c.988G>T	ENSP00000355292.5:p.Glu330Ter
ENST00000368297.5:c.745G>T	ENSP00000357280.1:p.Glu249Ter
ENST00000368298.2:n.252G>T
ENST00000368299.7:c.988G>T	ENSP00000357282.3:p.Glu330Ter
ENST00000368300.8:c.988G>T	ENSP00000357283.4:p.Glu330Ter
ENST00000368301.6:c.988G>T	ENSP00000357284.2:p.Glu330Ter
ENST00000448611.6:c.652G>T	ENSP00000395597.2:p.Glu218Ter
ENST00000473598.6:c.691G>T	ENSP00000421821.1:p.Glu231Ter
ENST00000496738.5:n.373G>T
ENST00000498722.2:n.220G>T
NM_001257374.2:c.652G>T	NP_001244303.1:p.Glu218Ter
NM_001282624.1:c.745G>T	NP_001269553.1:p.Glu249Ter
NM_001282625.1:c.988G>T	NP_001269554.1:p.Glu330Ter
NM_001282626.1:c.988G>T	NP_001269555.1:p.Glu330Ter
NM_005572.3:c.988G>T , LRG_254t1:c.988G>T	NP_005563.1:p.Glu330Ter
NM_170707.3:c.988G>T	NP_733821.1:p.Glu330Ter
NM_170708.3:c.988G>T	NP_733822.1:p.Glu330Ter
XM_011509533.1:c.652G>T	XP_011507835.1:p.Glu218Ter
XM_011509534.1:c.364G>T	XP_011507836.1:p.Glu122Ter
XR_921781.1:n.1277G>T
XM_011509534.2:c.364G>T	XP_011507836.1:p.Glu122Ter
XR_921781.2:n.1275G>T
NM_170707.4:c.988G>T MANE Select	NP_733821.1:p.Glu330Ter
NM_001257374.3:c.652G>T	NP_001244303.1:p.Glu218Ter
NM_001282626.2:c.988G>T	NP_001269555.1:p.Glu330Ter
NM_001282624.2:c.745G>T	NP_001269553.1:p.Glu249Ter
NM_001282625.2:c.988G>T	NP_001269554.1:p.Glu330Ter
NM_005572.4:c.988G>T MANE Plus Clinical	NP_005563.1:p.Glu330Ter
NM_170708.4:c.988G>T	NP_733822.1:p.Glu330Ter