Canonical Allele Identifier: CA421069267

Gene: LMNA

Linked Data

• MyVariant Identifiers: chr1:g.156107450G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156137659G>C , CM000663.2:g.156137659G>C	GRCh38
NC_000001.10:g.156107450G>C , CM000663.1:g.156107450G>C	GRCh37
NC_000001.9:g.154374074G>C	NCBI36
NG_008692.2:g.60087G>C , LRG_254:g.60087G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000504687.7:c.1056G>C	ENSP00000426535.3:p.Val352=
ENST00000498722.3:n.846G>C
ENST00000682650.1:c.1608+427G>C	ENSP00000506904.1:n.1608+427G>C
ENST00000683032.1:c.1614G>C	ENSP00000506771.1:p.Val538=
ENST00000684195.1:c.1585G>C	ENSP00000508220.1:p.Gly529Arg
ENST00000361308.9:c.1614G>C	ENSP00000355292.6:p.Val538=
ENST00000368300.9:c.1614G>C MANE Select	ENSP00000357283.4:p.Val538=
ENST00000496738.6:n.2073G>C
ENST00000674518.1:c.*964G>C	ENSP00000502261.1:n.*964G>C
ENST00000674600.1:c.*1413G>C	ENSP00000501666.1:n.*1413G>C
ENST00000674720.1:c.*176G>C	ENSP00000502798.1:n.*176G>C
ENST00000675431.1:n.1307G>C
ENST00000675455.1:c.*1414G>C	ENSP00000501795.1:n.*1414G>C
ENST00000675667.1:c.1614G>C	ENSP00000501803.1:p.Val538=
ENST00000675874.1:c.*1085G>C	ENSP00000501851.1:n.*1085G>C
ENST00000675881.1:c.*625G>C	ENSP00000501670.1:n.*625G>C
ENST00000675939.1:c.1614G>C	ENSP00000502256.1:p.Val538=
ENST00000675989.1:n.2473G>C
ENST00000676208.1:c.*717G>C	ENSP00000502468.1:n.*717G>C
ENST00000676283.1:n.2410G>C
ENST00000676385.2:c.1608+427G>C	ENSP00000502091.1:n.1608+427G>C
ENST00000676434.1:c.*625G>C	ENSP00000501648.1:n.*625G>C
ENST00000677389.1:c.1614G>C MANE Plus Clinical	ENSP00000503633.1:p.Val538=
ENST00000347559.6:c.1608+427G>C	ENSP00000292304.3:n.1608+427G>C
ENST00000361308.8:c.1359G>C	ENSP00000355292.5:p.Val453=
ENST00000368297.5:c.1371G>C	ENSP00000357280.1:p.Val457=
ENST00000368299.7:c.1614G>C	ENSP00000357282.3:p.Val538=
ENST00000368300.8:c.1614G>C	ENSP00000357283.4:p.Val538=
ENST00000368301.6:c.1614G>C	ENSP00000357284.2:p.Val538=
ENST00000448611.6:c.1278G>C	ENSP00000395597.2:p.Val426=
ENST00000473598.6:c.1317G>C	ENSP00000421821.1:p.Val439=
ENST00000496738.5:n.1083G>C
ENST00000498722.2:n.846G>C
ENST00000506981.1:n.198G>C
ENST00000508500.1:c.486+427G>C	ENSP00000424977.1:n.486+427G>C
NM_001257374.2:c.1278G>C	NP_001244303.1:p.Val426=
NM_001282624.1:c.1371G>C	NP_001269553.1:p.Val457=
NM_001282625.1:c.1614G>C	NP_001269554.1:p.Val538=
NM_001282626.1:c.1614G>C	NP_001269555.1:p.Val538=
NM_005572.3:c.1614G>C , LRG_254t1:c.1614G>C	NP_005563.1:p.Val538=
NM_170707.3:c.1614G>C	NP_733821.1:p.Val538=
NM_170708.3:c.1608+427G>C	NP_733822.1:n.1608+427G>C
XM_011509533.1:c.1278G>C	XP_011507835.1:p.Val426=
XM_011509534.1:c.990G>C	XP_011507836.1:p.Val330=
XR_921781.1:n.1903G>C
XM_011509534.2:c.990G>C	XP_011507836.1:p.Val330=
XR_921781.2:n.1901G>C
NM_170707.4:c.1614G>C MANE Select	NP_733821.1:p.Val538=
NM_001257374.3:c.1278G>C	NP_001244303.1:p.Val426=
NM_001282626.2:c.1614G>C	NP_001269555.1:p.Val538=
NM_001282624.2:c.1371G>C	NP_001269553.1:p.Val457=
NM_001282625.2:c.1614G>C	NP_001269554.1:p.Val538=
NM_005572.4:c.1614G>C MANE Plus Clinical	NP_005563.1:p.Val538=
NM_170708.4:c.1608+427G>C	NP_733822.1:n.1608+427G>C