Canonical Allele Identifier: CA342827891

Gene: LMNA

Linked Data

• MyVariant Identifiers: chr1:g.156108496A>C (hg19) ; chr1:g.156138705A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156138705A>C , CM000663.2:g.156138705A>C	GRCh38
NC_000001.10:g.156108496A>C , CM000663.1:g.156108496A>C	GRCh37
NC_000001.9:g.154375120A>C	NCBI36
NG_008692.2:g.61133A>C , LRG_254:g.61133A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.1358A>C	ENSP00000426535.3:p.Asp453Ala
ENST00000682650.1:c.1826A>C	ENSP00000506904.1:p.Asp609Ala
ENST00000683032.1:c.1916A>C	ENSP00000506771.1:p.Asp639Ala
ENST00000683773.1:n.163+98A>C
ENST00000684195.1:c.*1008A>C	ENSP00000508220.1:n.*1008A>C
ENST00000361308.9:c.1916A>C	ENSP00000355292.6:p.Asp639Ala
ENST00000368300.9:c.1916A>C MANE Select	ENSP00000357283.4:p.Asp639Ala
ENST00000674518.1:c.*1266A>C	ENSP00000502261.1:n.*1266A>C
ENST00000674600.1:c.*1715A>C	ENSP00000501666.1:n.*1715A>C
ENST00000675455.1:c.*1716A>C	ENSP00000501795.1:n.*1716A>C
ENST00000675667.1:c.1916A>C	ENSP00000501803.1:p.Asp639Ala
ENST00000675874.1:c.*1387A>C	ENSP00000501851.1:n.*1387A>C
ENST00000675881.1:c.*927A>C	ENSP00000501670.1:n.*927A>C
ENST00000675939.1:c.1916A>C	ENSP00000502256.1:p.Asp639Ala
ENST00000675989.1:n.3519A>C
ENST00000676208.1:c.*1019A>C	ENSP00000502468.1:n.*1019A>C
ENST00000676385.2:c.1826A>C	ENSP00000502091.1:p.Asp609Ala
ENST00000676434.1:c.*1671A>C	ENSP00000501648.1:n.*1671A>C
ENST00000347559.6:c.1826A>C	ENSP00000292304.3:p.Asp609Ala
ENST00000368299.7:c.1818+98A>C	ENSP00000357282.3:n.1818+98A>C
ENST00000368300.8:c.1916A>C	ENSP00000357283.4:p.Asp639Ala
ENST00000448611.6:c.1580A>C	ENSP00000395597.2:p.Asp527Ala
ENST00000473598.6:c.1619A>C	ENSP00000421821.1:p.Asp540Ala
ENST00000496738.5:n.2129A>C
ENST00000506981.1:n.500A>C
ENST00000508500.1:c.704A>C	ENSP00000424977.1:p.Asp235Ala
NM_001257374.2:c.1580A>C	NP_001244303.1:p.Asp527Ala
NM_001282626.1:c.1818+98A>C	NP_001269555.1:n.1818+98A>C
NM_170707.3:c.1916A>C	NP_733821.1:p.Asp639Ala
NM_170708.3:c.1826A>C	NP_733822.1:p.Asp609Ala
XM_011509533.1:c.1580A>C	XP_011507835.1:p.Asp527Ala
XM_011509534.1:c.1292A>C	XP_011507836.1:p.Asp431Ala
XR_921781.1:n.2205A>C
XM_011509534.2:c.1292A>C	XP_011507836.1:p.Asp431Ala
XR_921781.2:n.2203A>C
NM_170707.4:c.1916A>C MANE Select	NP_733821.1:p.Asp639Ala
NM_001257374.3:c.1580A>C	NP_001244303.1:p.Asp527Ala
NM_001282626.2:c.1818+98A>C	NP_001269555.1:n.1818+98A>C
NM_170708.4:c.1826A>C	NP_733822.1:p.Asp609Ala