Canonical Allele Identifier: CA342817319

Gene: LMNA

Linked Data

• ClinVar Variation Id: 2773538
• ClinVar RCV Id: RCV003532555
• MyVariant Identifiers: chr1:g.156104707C>A (hg19) ; chr1:g.156134916C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156134916C>A , CM000663.2:g.156134916C>A	GRCh38
NC_000001.10:g.156104707C>A , CM000663.1:g.156104707C>A	GRCh37
NC_000001.9:g.154371331C>A	NCBI36
NG_008692.2:g.57344C>A , LRG_254:g.57344C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.193C>A	ENSP00000426535.3:p.Gln65Lys
ENST00000682650.1:c.751C>A	ENSP00000506904.1:p.Gln251Lys
ENST00000683032.1:c.751C>A	ENSP00000506771.1:p.Gln251Lys
ENST00000684195.1:c.751C>A	ENSP00000508220.1:p.Gln251Lys
ENST00000361308.9:c.751C>A	ENSP00000355292.6:p.Gln251Lys
ENST00000368300.9:c.751C>A MANE Select	ENSP00000357283.4:p.Gln251Lys
ENST00000496738.6:n.1126C>A
ENST00000504687.6:c.87C>A	ENSP00000426535.2:p.Pro29=
ENST00000674518.1:c.*101C>A	ENSP00000502261.1:n.*101C>A
ENST00000674600.1:c.*550C>A	ENSP00000501666.1:n.*550C>A
ENST00000674720.1:c.751C>A	ENSP00000502798.1:p.Gln251Lys
ENST00000675431.1:n.444C>A
ENST00000675455.1:c.*551C>A	ENSP00000501795.1:n.*551C>A
ENST00000675667.1:c.751C>A	ENSP00000501803.1:p.Gln251Lys
ENST00000675874.1:c.*222C>A	ENSP00000501851.1:n.*222C>A
ENST00000675881.1:c.751C>A	ENSP00000501670.1:p.Gln251Lys
ENST00000675939.1:c.751C>A	ENSP00000502256.1:p.Gln251Lys
ENST00000675989.1:n.1126C>A
ENST00000676208.1:c.751C>A	ENSP00000502468.1:p.Gln251Lys
ENST00000676283.1:n.1126C>A
ENST00000676385.2:c.751C>A	ENSP00000502091.1:p.Gln251Lys
ENST00000676434.1:c.751C>A	ENSP00000501648.1:p.Gln251Lys
ENST00000677389.1:c.751C>A MANE Plus Clinical	ENSP00000503633.1:p.Gln251Lys
ENST00000347559.6:c.751C>A	ENSP00000292304.3:p.Gln251Lys
ENST00000361308.8:c.751C>A	ENSP00000355292.5:p.Gln251Lys
ENST00000368297.5:c.508C>A	ENSP00000357280.1:p.Gln170Lys
ENST00000368299.7:c.751C>A	ENSP00000357282.3:p.Gln251Lys
ENST00000368300.8:c.751C>A	ENSP00000357283.4:p.Gln251Lys
ENST00000368301.6:c.751C>A	ENSP00000357284.2:p.Gln251Lys
ENST00000448611.6:c.415C>A	ENSP00000395597.2:p.Gln139Lys
ENST00000473598.6:c.454C>A	ENSP00000421821.1:p.Gln152Lys
ENST00000496738.5:n.96C>A
ENST00000504687.5:c.502C>A	ENSP00000426535.1:p.Gln168Lys
ENST00000515459.5:c.*425C>A	ENSP00000424518.1:n.*425C>A
ENST00000515824.1:n.112C>A
NM_001257374.2:c.415C>A	NP_001244303.1:p.Gln139Lys
NM_001282624.1:c.508C>A	NP_001269553.1:p.Gln170Lys
NM_001282625.1:c.751C>A	NP_001269554.1:p.Gln251Lys
NM_001282626.1:c.751C>A	NP_001269555.1:p.Gln251Lys
NM_005572.3:c.751C>A , LRG_254t1:c.751C>A	NP_005563.1:p.Gln251Lys
NM_170707.3:c.751C>A	NP_733821.1:p.Gln251Lys
NM_170708.3:c.751C>A	NP_733822.1:p.Gln251Lys
XM_011509533.1:c.415C>A	XP_011507835.1:p.Gln139Lys
XM_011509534.1:c.87C>A	XP_011507836.1:p.Pro29=
XR_921781.1:n.1000C>A
XM_011509534.2:c.87C>A	XP_011507836.1:p.Pro29=
XR_921781.2:n.998C>A
NM_170707.4:c.751C>A MANE Select	NP_733821.1:p.Gln251Lys
NM_001257374.3:c.415C>A	NP_001244303.1:p.Gln139Lys
NM_001282626.2:c.751C>A	NP_001269555.1:p.Gln251Lys
NM_001282624.2:c.508C>A	NP_001269553.1:p.Gln170Lys
NM_001282625.2:c.751C>A	NP_001269554.1:p.Gln251Lys
NM_005572.4:c.751C>A MANE Plus Clinical	NP_005563.1:p.Gln251Lys
NM_170708.4:c.751C>A	NP_733822.1:p.Gln251Lys