Canonical Allele Identifier: CA421257823

Gene: LMNA

Linked Data

• MyVariant Identifiers: chr1:g.156105841T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156136050T>C , CM000663.2:g.156136050T>C	GRCh38
NC_000001.10:g.156105841T>C , CM000663.1:g.156105841T>C	GRCh37
NC_000001.9:g.154372465T>C	NCBI36
NG_008692.2:g.58478T>C , LRG_254:g.58478T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000504687.7:c.528T>C	ENSP00000426535.3:p.Leu176=
ENST00000498722.3:n.318T>C
ENST00000682650.1:c.1086T>C	ENSP00000506904.1:p.Leu362=
ENST00000683032.1:c.1086T>C	ENSP00000506771.1:p.Leu362=
ENST00000684195.1:c.1086T>C	ENSP00000508220.1:p.Leu362=
ENST00000361308.9:c.1086T>C	ENSP00000355292.6:p.Leu362=
ENST00000368300.9:c.1086T>C MANE Select	ENSP00000357283.4:p.Leu362=
ENST00000496738.6:n.1461T>C
ENST00000674518.1:c.*436T>C	ENSP00000502261.1:n.*436T>C
ENST00000674600.1:c.*885T>C	ENSP00000501666.1:n.*885T>C
ENST00000674720.1:c.1086T>C	ENSP00000502798.1:p.Leu362=
ENST00000675431.1:n.779T>C
ENST00000675455.1:c.*886T>C	ENSP00000501795.1:n.*886T>C
ENST00000675667.1:c.1086T>C	ENSP00000501803.1:p.Leu362=
ENST00000675874.1:c.*557T>C	ENSP00000501851.1:n.*557T>C
ENST00000675881.1:c.*97T>C	ENSP00000501670.1:n.*97T>C
ENST00000675939.1:c.1086T>C	ENSP00000502256.1:p.Leu362=
ENST00000675989.1:n.1461T>C
ENST00000676208.1:c.*97T>C	ENSP00000502468.1:n.*97T>C
ENST00000676283.1:n.1461T>C
ENST00000676385.2:c.1086T>C	ENSP00000502091.1:p.Leu362=
ENST00000676434.1:c.*97T>C	ENSP00000501648.1:n.*97T>C
ENST00000677389.1:c.1086T>C MANE Plus Clinical	ENSP00000503633.1:p.Leu362=
ENST00000347559.6:c.1086T>C	ENSP00000292304.3:p.Leu362=
ENST00000361308.8:c.1086T>C	ENSP00000355292.5:p.Leu362=
ENST00000368297.5:c.843T>C	ENSP00000357280.1:p.Leu281=
ENST00000368298.2:n.350T>C
ENST00000368299.7:c.1086T>C	ENSP00000357282.3:p.Leu362=
ENST00000368300.8:c.1086T>C	ENSP00000357283.4:p.Leu362=
ENST00000368301.6:c.1086T>C	ENSP00000357284.2:p.Leu362=
ENST00000448611.6:c.750T>C	ENSP00000395597.2:p.Leu250=
ENST00000473598.6:c.789T>C	ENSP00000421821.1:p.Leu263=
ENST00000496738.5:n.471T>C
ENST00000498722.2:n.318T>C
NM_001257374.2:c.750T>C	NP_001244303.1:p.Leu250=
NM_001282624.1:c.843T>C	NP_001269553.1:p.Leu281=
NM_001282625.1:c.1086T>C	NP_001269554.1:p.Leu362=
NM_001282626.1:c.1086T>C	NP_001269555.1:p.Leu362=
NM_005572.3:c.1086T>C , LRG_254t1:c.1086T>C	NP_005563.1:p.Leu362=
NM_170707.3:c.1086T>C	NP_733821.1:p.Leu362=
NM_170708.3:c.1086T>C	NP_733822.1:p.Leu362=
XM_011509533.1:c.750T>C	XP_011507835.1:p.Leu250=
XM_011509534.1:c.462T>C	XP_011507836.1:p.Leu154=
XR_921781.1:n.1375T>C
XM_011509534.2:c.462T>C	XP_011507836.1:p.Leu154=
XR_921781.2:n.1373T>C
NM_170707.4:c.1086T>C MANE Select	NP_733821.1:p.Leu362=
NM_001257374.3:c.750T>C	NP_001244303.1:p.Leu250=
NM_001282626.2:c.1086T>C	NP_001269555.1:p.Leu362=
NM_001282624.2:c.843T>C	NP_001269553.1:p.Leu281=
NM_001282625.2:c.1086T>C	NP_001269554.1:p.Leu362=
NM_005572.4:c.1086T>C MANE Plus Clinical	NP_005563.1:p.Leu362=
NM_170708.4:c.1086T>C	NP_733822.1:p.Leu362=