Canonical Allele Identifier: CA342823343

Gene: LMNA

Linked Data

• ClinVar Variation Id: 476824
• ClinVar RCV Id: RCV000540642
• dbSNP Id: rs267607557
• MyVariant Identifiers: chr1:g.156106973T>C (hg19) ; chr1:g.156137182T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156137182T>C , CM000663.2:g.156137182T>C	GRCh38
NC_000001.10:g.156106973T>C , CM000663.1:g.156106973T>C	GRCh37
NC_000001.9:g.154373597T>C	NCBI36
NG_008692.2:g.59610T>C , LRG_254:g.59610T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.1000T>C	ENSP00000426535.3:p.Trp334Arg
ENST00000459904.2:n.806T>C
ENST00000498722.3:n.790T>C
ENST00000682650.1:c.1558T>C	ENSP00000506904.1:p.Trp520Arg
ENST00000683032.1:c.1558T>C	ENSP00000506771.1:p.Trp520Arg
ENST00000684195.1:c.1558T>C	ENSP00000508220.1:p.Trp520Arg
ENST00000361308.9:c.1558T>C	ENSP00000355292.6:p.Trp520Arg
ENST00000368300.9:c.1558T>C MANE Select	ENSP00000357283.4:p.Trp520Arg
ENST00000496738.6:n.2017T>C
ENST00000674518.1:c.*908T>C	ENSP00000502261.1:n.*908T>C
ENST00000674600.1:c.*1357T>C	ENSP00000501666.1:n.*1357T>C
ENST00000674720.1:c.*120T>C	ENSP00000502798.1:n.*120T>C
ENST00000675431.1:n.1251T>C
ENST00000675455.1:c.*1358T>C	ENSP00000501795.1:n.*1358T>C
ENST00000675667.1:c.1558T>C	ENSP00000501803.1:p.Trp520Arg
ENST00000675874.1:c.*1029T>C	ENSP00000501851.1:n.*1029T>C
ENST00000675881.1:c.*569T>C	ENSP00000501670.1:n.*569T>C
ENST00000675939.1:c.1558T>C	ENSP00000502256.1:p.Trp520Arg
ENST00000675989.1:n.2417T>C
ENST00000676208.1:c.*661T>C	ENSP00000502468.1:n.*661T>C
ENST00000676283.1:n.1933T>C
ENST00000676385.2:c.1558T>C	ENSP00000502091.1:p.Trp520Arg
ENST00000676434.1:c.*569T>C	ENSP00000501648.1:n.*569T>C
ENST00000677389.1:c.1558T>C MANE Plus Clinical	ENSP00000503633.1:p.Trp520Arg
ENST00000347559.6:c.1558T>C	ENSP00000292304.3:p.Trp520Arg
ENST00000361308.8:c.1312-9T>C	ENSP00000355292.5:n.1312-9T>C
ENST00000368297.5:c.1315T>C	ENSP00000357280.1:p.Trp439Arg
ENST00000368298.2:n.1390T>C
ENST00000368299.7:c.1558T>C	ENSP00000357282.3:p.Trp520Arg
ENST00000368300.8:c.1558T>C	ENSP00000357283.4:p.Trp520Arg
ENST00000368301.6:c.1558T>C	ENSP00000357284.2:p.Trp520Arg
ENST00000448611.6:c.1222T>C	ENSP00000395597.2:p.Trp408Arg
ENST00000459904.1:n.806T>C
ENST00000473598.6:c.1261T>C	ENSP00000421821.1:p.Trp421Arg
ENST00000496738.5:n.1027T>C
ENST00000498722.2:n.790T>C
ENST00000508500.1:c.436T>C	ENSP00000424977.1:p.Trp146Arg
NM_001257374.2:c.1222T>C	NP_001244303.1:p.Trp408Arg
NM_001282624.1:c.1315T>C	NP_001269553.1:p.Trp439Arg
NM_001282625.1:c.1558T>C	NP_001269554.1:p.Trp520Arg
NM_001282626.1:c.1558T>C	NP_001269555.1:p.Trp520Arg
NM_005572.3:c.1558T>C , LRG_254t1:c.1558T>C	NP_005563.1:p.Trp520Arg
NM_170707.3:c.1558T>C	NP_733821.1:p.Trp520Arg
NM_170708.3:c.1558T>C	NP_733822.1:p.Trp520Arg
XM_011509533.1:c.1222T>C	XP_011507835.1:p.Trp408Arg
XM_011509534.1:c.934T>C	XP_011507836.1:p.Trp312Arg
XR_921781.1:n.1847T>C
XM_011509534.2:c.934T>C	XP_011507836.1:p.Trp312Arg
XR_921781.2:n.1845T>C
NM_170707.4:c.1558T>C MANE Select	NP_733821.1:p.Trp520Arg
NM_001257374.3:c.1222T>C	NP_001244303.1:p.Trp408Arg
NM_001282626.2:c.1558T>C	NP_001269555.1:p.Trp520Arg
NM_001282624.2:c.1315T>C	NP_001269553.1:p.Trp439Arg
NM_001282625.2:c.1558T>C	NP_001269554.1:p.Trp520Arg
NM_005572.4:c.1558T>C MANE Plus Clinical	NP_005563.1:p.Trp520Arg
NM_170708.4:c.1558T>C	NP_733822.1:p.Trp520Arg