Canonical Allele Identifier: CA658795531

Gene: LMNA

Linked Data

• ClinVar Variation Id: 510751
• ClinVar RCV Id: RCV000612522
• dbSNP Id: rs1553265425
• MyVariant Identifiers: chr1:g.156104960del (hg19) ; chr1:g.156135169del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156135169del , CM000663.2:g.156135169del	GRCh38
NC_000001.10:g.156104960del , CM000663.1:g.156104960del	GRCh37
NC_000001.9:g.154371584del	NCBI36
NG_008692.2:g.57597del , LRG_254:g.57597del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.253-18del	ENSP00000426535.3:n.253-18del
ENST00000682650.1:c.811-18del	ENSP00000506904.1:n.811-18del
ENST00000683032.1:c.811-18del	ENSP00000506771.1:n.811-18del
ENST00000684195.1:c.811-18del	ENSP00000508220.1:n.811-18del
ENST00000361308.9:c.811-18del	ENSP00000355292.6:n.811-18del
ENST00000368300.9:c.811-18del MANE Select	ENSP00000357283.4:n.811-18del
ENST00000496738.6:n.1186-18del
ENST00000674518.1:c.*161-18del	ENSP00000502261.1:n.*161-18del
ENST00000674600.1:c.*610-18del	ENSP00000501666.1:n.*610-18del
ENST00000674720.1:c.811-18del	ENSP00000502798.1:n.811-18del
ENST00000675431.1:n.504-18del
ENST00000675455.1:c.*611-18del	ENSP00000501795.1:n.*611-18del
ENST00000675667.1:c.811-18del	ENSP00000501803.1:n.811-18del
ENST00000675874.1:c.*282-18del	ENSP00000501851.1:n.*282-18del
ENST00000675881.1:c.811-18del	ENSP00000501670.1:n.811-18del
ENST00000675939.1:c.811-18del	ENSP00000502256.1:n.811-18del
ENST00000675989.1:n.1186-18del
ENST00000676208.1:c.811-18del	ENSP00000502468.1:n.811-18del
ENST00000676283.1:n.1186-18del
ENST00000676385.2:c.811-18del	ENSP00000502091.1:n.811-18del
ENST00000676434.1:c.811-18del	ENSP00000501648.1:n.811-18del
ENST00000677389.1:c.811-18del MANE Plus Clinical	ENSP00000503633.1:n.811-18del
ENST00000347559.6:c.811-18del	ENSP00000292304.3:n.811-18del
ENST00000361308.8:c.811-18del	ENSP00000355292.5:n.811-18del
ENST00000368297.5:c.568-18del	ENSP00000357280.1:n.568-18del
ENST00000368298.2:n.57del
ENST00000368299.7:c.811-18del	ENSP00000357282.3:n.811-18del
ENST00000368300.8:c.811-18del	ENSP00000357283.4:n.811-18del
ENST00000368301.6:c.811-18del	ENSP00000357284.2:n.811-18del
ENST00000448611.6:c.475-18del	ENSP00000395597.2:n.475-18del
ENST00000473598.6:c.514-18del	ENSP00000421821.1:n.514-18del
ENST00000496738.5:n.156-18del
ENST00000515459.5:c.*485-18del	ENSP00000424518.1:n.*485-18del
ENST00000515824.1:n.172-18del
NM_001257374.2:c.475-18del	NP_001244303.1:n.475-18del
NM_001282624.1:c.568-18del	NP_001269553.1:n.568-18del
NM_001282625.1:c.811-18del	NP_001269554.1:n.811-18del
NM_001282626.1:c.811-18del	NP_001269555.1:n.811-18del
NM_005572.3:c.811-18del , LRG_254t1:c.811-18del	NP_005563.1:n.811-18del
NM_170707.3:c.811-18del	NP_733821.1:n.811-18del
NM_170708.3:c.811-18del	NP_733822.1:n.811-18del
XM_011509533.1:c.475-18del	XP_011507835.1:n.475-18del
XM_011509534.1:c.147-18del	XP_011507836.1:n.147-18del
XR_921781.1:n.1060-18del
XM_011509534.2:c.147-18del	XP_011507836.1:n.147-18del
XR_921781.2:n.1058-18del
NM_170707.4:c.811-18del MANE Select	NP_733821.1:n.811-18del
NM_001257374.3:c.475-18del	NP_001244303.1:n.475-18del
NM_001282626.2:c.811-18del	NP_001269555.1:n.811-18del
NM_001282624.2:c.568-18del	NP_001269553.1:n.568-18del
NM_001282625.2:c.811-18del	NP_001269554.1:n.811-18del
NM_005572.4:c.811-18del MANE Plus Clinical	NP_005563.1:n.811-18del
NM_170708.4:c.811-18del	NP_733822.1:n.811-18del