Canonical Allele Identifier: CA342817124

Gene: LMNA

Linked Data

• MyVariant Identifiers: chr1:g.156104602C>A (hg19) ; chr1:g.156134811C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156134811C>A , CM000663.2:g.156134811C>A	GRCh38
NC_000001.10:g.156104602C>A , CM000663.1:g.156104602C>A	GRCh37
NC_000001.9:g.154371226C>A	NCBI36
NG_008692.2:g.57239C>A , LRG_254:g.57239C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000504687.7:c.88C>A	ENSP00000426535.3:p.Arg30Ser
ENST00000682650.1:c.646C>A	ENSP00000506904.1:p.Arg216Ser
ENST00000683032.1:c.646C>A	ENSP00000506771.1:p.Arg216Ser
ENST00000684195.1:c.646C>A	ENSP00000508220.1:p.Arg216Ser
ENST00000361308.9:c.646C>A	ENSP00000355292.6:p.Arg216Ser
ENST00000368300.9:c.646C>A MANE Select	ENSP00000357283.4:p.Arg216Ser
ENST00000496738.6:n.1021C>A
ENST00000504687.6:c.-19C>A	ENSP00000426535.2:n.-19C>A
ENST00000674518.1:c.641C>A	ENSP00000502261.1:p.Ala214Glu
ENST00000674600.1:c.*445C>A	ENSP00000501666.1:n.*445C>A
ENST00000674720.1:c.646C>A	ENSP00000502798.1:p.Arg216Ser
ENST00000675431.1:n.339C>A
ENST00000675455.1:c.*446C>A	ENSP00000501795.1:n.*446C>A
ENST00000675667.1:c.646C>A	ENSP00000501803.1:p.Arg216Ser
ENST00000675874.1:c.*117C>A	ENSP00000501851.1:n.*117C>A
ENST00000675881.1:c.646C>A	ENSP00000501670.1:p.Arg216Ser
ENST00000675939.1:c.646C>A	ENSP00000502256.1:p.Arg216Ser
ENST00000675989.1:n.1021C>A
ENST00000676208.1:c.646C>A	ENSP00000502468.1:p.Arg216Ser
ENST00000676283.1:n.1021C>A
ENST00000676385.2:c.646C>A	ENSP00000502091.1:p.Arg216Ser
ENST00000676434.1:c.646C>A	ENSP00000501648.1:p.Arg216Ser
ENST00000677389.1:c.646C>A MANE Plus Clinical	ENSP00000503633.1:p.Arg216Ser
ENST00000347559.6:c.646C>A	ENSP00000292304.3:p.Arg216Ser
ENST00000361308.8:c.646C>A	ENSP00000355292.5:p.Arg216Ser
ENST00000368297.5:c.403C>A	ENSP00000357280.1:p.Arg135Ser
ENST00000368299.7:c.646C>A	ENSP00000357282.3:p.Arg216Ser
ENST00000368300.8:c.646C>A	ENSP00000357283.4:p.Arg216Ser
ENST00000368301.6:c.646C>A	ENSP00000357284.2:p.Arg216Ser
ENST00000448611.6:c.310C>A	ENSP00000395597.2:p.Arg104Ser
ENST00000473598.6:c.349C>A	ENSP00000421821.1:p.Arg117Ser
ENST00000504687.5:c.397C>A	ENSP00000426535.1:p.Arg133Ser
ENST00000515459.5:c.*320C>A	ENSP00000424518.1:n.*320C>A
ENST00000515824.1:n.7C>A
NM_001257374.2:c.310C>A	NP_001244303.1:p.Arg104Ser
NM_001282624.1:c.403C>A	NP_001269553.1:p.Arg135Ser
NM_001282625.1:c.646C>A	NP_001269554.1:p.Arg216Ser
NM_001282626.1:c.646C>A	NP_001269555.1:p.Arg216Ser
NM_005572.3:c.646C>A , LRG_254t1:c.646C>A	NP_005563.1:p.Arg216Ser
NM_170707.3:c.646C>A	NP_733821.1:p.Arg216Ser
NM_170708.3:c.646C>A	NP_733822.1:p.Arg216Ser
XM_011509533.1:c.310C>A	XP_011507835.1:p.Arg104Ser
XM_011509534.1:c.-19C>A	XP_011507836.1:n.-19C>A
XR_921781.1:n.895C>A
XM_011509534.2:c.-19C>A	XP_011507836.1:n.-19C>A
XR_921781.2:n.893C>A
NM_170707.4:c.646C>A MANE Select	NP_733821.1:p.Arg216Ser
NM_001257374.3:c.310C>A	NP_001244303.1:p.Arg104Ser
NM_001282626.2:c.646C>A	NP_001269555.1:p.Arg216Ser
NM_001282624.2:c.403C>A	NP_001269553.1:p.Arg135Ser
NM_001282625.2:c.646C>A	NP_001269554.1:p.Arg216Ser
NM_005572.4:c.646C>A MANE Plus Clinical	NP_005563.1:p.Arg216Ser
NM_170708.4:c.646C>A	NP_733822.1:p.Arg216Ser