Canonical Allele Identifier: CA342817332

Gene: LMNA

Linked Data

• ClinVar Variation Id: 597500
• ClinVar RCV Id: RCV000733645
• dbSNP Id: rs1558129589
• MyVariant Identifiers: chr1:g.156104711A>C (hg19) ; chr1:g.156134920A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156134920A>C , CM000663.2:g.156134920A>C	GRCh38
NC_000001.10:g.156104711A>C , CM000663.1:g.156104711A>C	GRCh37
NC_000001.9:g.154371335A>C	NCBI36
NG_008692.2:g.57348A>C , LRG_254:g.57348A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000504687.7:c.197A>C	ENSP00000426535.3:p.His66Pro
ENST00000682650.1:c.755A>C	ENSP00000506904.1:p.His252Pro
ENST00000683032.1:c.755A>C	ENSP00000506771.1:p.His252Pro
ENST00000684195.1:c.755A>C	ENSP00000508220.1:p.His252Pro
ENST00000361308.9:c.755A>C	ENSP00000355292.6:p.His252Pro
ENST00000368300.9:c.755A>C MANE Select	ENSP00000357283.4:p.His252Pro
ENST00000496738.6:n.1130A>C
ENST00000504687.6:c.91A>C	ENSP00000426535.2:p.Met31Leu
ENST00000674518.1:c.*105A>C	ENSP00000502261.1:n.*105A>C
ENST00000674600.1:c.*554A>C	ENSP00000501666.1:n.*554A>C
ENST00000674720.1:c.755A>C	ENSP00000502798.1:p.His252Pro
ENST00000675431.1:n.448A>C
ENST00000675455.1:c.*555A>C	ENSP00000501795.1:n.*555A>C
ENST00000675667.1:c.755A>C	ENSP00000501803.1:p.His252Pro
ENST00000675874.1:c.*226A>C	ENSP00000501851.1:n.*226A>C
ENST00000675881.1:c.755A>C	ENSP00000501670.1:p.His252Pro
ENST00000675939.1:c.755A>C	ENSP00000502256.1:p.His252Pro
ENST00000675989.1:n.1130A>C
ENST00000676208.1:c.755A>C	ENSP00000502468.1:p.His252Pro
ENST00000676283.1:n.1130A>C
ENST00000676385.2:c.755A>C	ENSP00000502091.1:p.His252Pro
ENST00000676434.1:c.755A>C	ENSP00000501648.1:p.His252Pro
ENST00000677389.1:c.755A>C MANE Plus Clinical	ENSP00000503633.1:p.His252Pro
ENST00000347559.6:c.755A>C	ENSP00000292304.3:p.His252Pro
ENST00000361308.8:c.755A>C	ENSP00000355292.5:p.His252Pro
ENST00000368297.5:c.512A>C	ENSP00000357280.1:p.His171Pro
ENST00000368299.7:c.755A>C	ENSP00000357282.3:p.His252Pro
ENST00000368300.8:c.755A>C	ENSP00000357283.4:p.His252Pro
ENST00000368301.6:c.755A>C	ENSP00000357284.2:p.His252Pro
ENST00000448611.6:c.419A>C	ENSP00000395597.2:p.His140Pro
ENST00000473598.6:c.458A>C	ENSP00000421821.1:p.His153Pro
ENST00000496738.5:n.100A>C
ENST00000504687.5:c.506A>C	ENSP00000426535.1:p.His169Pro
ENST00000515459.5:c.*429A>C	ENSP00000424518.1:n.*429A>C
ENST00000515824.1:n.116A>C
NM_001257374.2:c.419A>C	NP_001244303.1:p.His140Pro
NM_001282624.1:c.512A>C	NP_001269553.1:p.His171Pro
NM_001282625.1:c.755A>C	NP_001269554.1:p.His252Pro
NM_001282626.1:c.755A>C	NP_001269555.1:p.His252Pro
NM_005572.3:c.755A>C , LRG_254t1:c.755A>C	NP_005563.1:p.His252Pro
NM_170707.3:c.755A>C	NP_733821.1:p.His252Pro
NM_170708.3:c.755A>C	NP_733822.1:p.His252Pro
XM_011509533.1:c.419A>C	XP_011507835.1:p.His140Pro
XM_011509534.1:c.91A>C	XP_011507836.1:p.Met31Leu
XR_921781.1:n.1004A>C
XM_011509534.2:c.91A>C	XP_011507836.1:p.Met31Leu
XR_921781.2:n.1002A>C
NM_170707.4:c.755A>C MANE Select	NP_733821.1:p.His252Pro
NM_001257374.3:c.419A>C	NP_001244303.1:p.His140Pro
NM_001282626.2:c.755A>C	NP_001269555.1:p.His252Pro
NM_001282624.2:c.512A>C	NP_001269553.1:p.His171Pro
NM_001282625.2:c.755A>C	NP_001269554.1:p.His252Pro
NM_005572.4:c.755A>C MANE Plus Clinical	NP_005563.1:p.His252Pro
NM_170708.4:c.755A>C	NP_733822.1:p.His252Pro