Canonical Allele Identifier: CA342822983

Gene: LMNA

Linked Data

• MyVariant Identifiers: chr1:g.156106911C>T (hg19) ; chr1:g.156137120C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156137120C>T , CM000663.2:g.156137120C>T	GRCh38
NC_000001.10:g.156106911C>T , CM000663.1:g.156106911C>T	GRCh37
NC_000001.9:g.154373535C>T	NCBI36
NG_008692.2:g.59548C>T , LRG_254:g.59548C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000504687.7:c.938C>T	ENSP00000426535.3:p.Ala313Val
ENST00000459904.2:n.744C>T
ENST00000498722.3:n.728C>T
ENST00000682650.1:c.1496C>T	ENSP00000506904.1:p.Ala499Val
ENST00000683032.1:c.1496C>T	ENSP00000506771.1:p.Ala499Val
ENST00000684195.1:c.1496C>T	ENSP00000508220.1:p.Ala499Val
ENST00000361308.9:c.1496C>T	ENSP00000355292.6:p.Ala499Val
ENST00000368300.9:c.1496C>T MANE Select	ENSP00000357283.4:p.Ala499Val
ENST00000496738.6:n.1955C>T
ENST00000674518.1:c.*846C>T	ENSP00000502261.1:n.*846C>T
ENST00000674600.1:c.*1295C>T	ENSP00000501666.1:n.*1295C>T
ENST00000674720.1:c.*58C>T	ENSP00000502798.1:n.*58C>T
ENST00000675431.1:n.1189C>T
ENST00000675455.1:c.*1296C>T	ENSP00000501795.1:n.*1296C>T
ENST00000675667.1:c.1496C>T	ENSP00000501803.1:p.Ala499Val
ENST00000675874.1:c.*967C>T	ENSP00000501851.1:n.*967C>T
ENST00000675881.1:c.*507C>T	ENSP00000501670.1:n.*507C>T
ENST00000675939.1:c.1496C>T	ENSP00000502256.1:p.Ala499Val
ENST00000675989.1:n.2355C>T
ENST00000676208.1:c.*599C>T	ENSP00000502468.1:n.*599C>T
ENST00000676283.1:n.1871C>T
ENST00000676385.2:c.1496C>T	ENSP00000502091.1:p.Ala499Val
ENST00000676434.1:c.*507C>T	ENSP00000501648.1:n.*507C>T
ENST00000677389.1:c.1496C>T MANE Plus Clinical	ENSP00000503633.1:p.Ala499Val
ENST00000347559.6:c.1496C>T	ENSP00000292304.3:p.Ala499Val
ENST00000361308.8:c.1312-71C>T	ENSP00000355292.5:n.1312-71C>T
ENST00000368297.5:c.1253C>T	ENSP00000357280.1:p.Ala418Val
ENST00000368298.2:n.1328C>T
ENST00000368299.7:c.1496C>T	ENSP00000357282.3:p.Ala499Val
ENST00000368300.8:c.1496C>T	ENSP00000357283.4:p.Ala499Val
ENST00000368301.6:c.1496C>T	ENSP00000357284.2:p.Ala499Val
ENST00000448611.6:c.1160C>T	ENSP00000395597.2:p.Ala387Val
ENST00000459904.1:n.744C>T
ENST00000473598.6:c.1199C>T	ENSP00000421821.1:p.Ala400Val
ENST00000496738.5:n.965C>T
ENST00000498722.2:n.728C>T
ENST00000508500.1:c.374C>T	ENSP00000424977.1:p.Ala125Val
NM_001257374.2:c.1160C>T	NP_001244303.1:p.Ala387Val
NM_001282624.1:c.1253C>T	NP_001269553.1:p.Ala418Val
NM_001282625.1:c.1496C>T	NP_001269554.1:p.Ala499Val
NM_001282626.1:c.1496C>T	NP_001269555.1:p.Ala499Val
NM_005572.3:c.1496C>T , LRG_254t1:c.1496C>T	NP_005563.1:p.Ala499Val
NM_170707.3:c.1496C>T	NP_733821.1:p.Ala499Val
NM_170708.3:c.1496C>T	NP_733822.1:p.Ala499Val
XM_011509533.1:c.1160C>T	XP_011507835.1:p.Ala387Val
XM_011509534.1:c.872C>T	XP_011507836.1:p.Ala291Val
XR_921781.1:n.1785C>T
XM_011509534.2:c.872C>T	XP_011507836.1:p.Ala291Val
XR_921781.2:n.1783C>T
NM_170707.4:c.1496C>T MANE Select	NP_733821.1:p.Ala499Val
NM_001257374.3:c.1160C>T	NP_001244303.1:p.Ala387Val
NM_001282626.2:c.1496C>T	NP_001269555.1:p.Ala499Val
NM_001282624.2:c.1253C>T	NP_001269553.1:p.Ala418Val
NM_001282625.2:c.1496C>T	NP_001269554.1:p.Ala499Val
NM_005572.4:c.1496C>T MANE Plus Clinical	NP_005563.1:p.Ala499Val
NM_170708.4:c.1496C>T	NP_733822.1:p.Ala499Val