Canonical Allele Identifier: CA342825692

Gene: LMNA

Linked Data

• MyVariant Identifiers: chr1:g.156107507T>G (hg19) ; chr1:g.156137716T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156137716T>G , CM000663.2:g.156137716T>G	GRCh38
NC_000001.10:g.156107507T>G , CM000663.1:g.156107507T>G	GRCh37
NC_000001.9:g.154374131T>G	NCBI36
NG_008692.2:g.60144T>G , LRG_254:g.60144T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.1113T>G	ENSP00000426535.3:p.Asp371Glu
ENST00000498722.3:n.903T>G
ENST00000682650.1:c.1608+484T>G	ENSP00000506904.1:n.1608+484T>G
ENST00000683032.1:c.1671T>G	ENSP00000506771.1:p.Asp557Glu
ENST00000683773.1:n.16T>G
ENST00000684195.1:c.*19T>G	ENSP00000508220.1:n.*19T>G
ENST00000361308.9:c.1671T>G	ENSP00000355292.6:p.Asp557Glu
ENST00000368300.9:c.1671T>G MANE Select	ENSP00000357283.4:p.Asp557Glu
ENST00000496738.6:n.2130T>G
ENST00000674518.1:c.*1021T>G	ENSP00000502261.1:n.*1021T>G
ENST00000674600.1:c.*1470T>G	ENSP00000501666.1:n.*1470T>G
ENST00000674720.1:c.*233T>G	ENSP00000502798.1:n.*233T>G
ENST00000675431.1:n.1364T>G
ENST00000675455.1:c.*1471T>G	ENSP00000501795.1:n.*1471T>G
ENST00000675667.1:c.1671T>G	ENSP00000501803.1:p.Asp557Glu
ENST00000675874.1:c.*1142T>G	ENSP00000501851.1:n.*1142T>G
ENST00000675881.1:c.*682T>G	ENSP00000501670.1:n.*682T>G
ENST00000675939.1:c.1671T>G	ENSP00000502256.1:p.Asp557Glu
ENST00000675989.1:n.2530T>G
ENST00000676208.1:c.*774T>G	ENSP00000502468.1:n.*774T>G
ENST00000676283.1:n.2467T>G
ENST00000676385.2:c.1608+484T>G	ENSP00000502091.1:n.1608+484T>G
ENST00000676434.1:c.*682T>G	ENSP00000501648.1:n.*682T>G
ENST00000677389.1:c.1671T>G MANE Plus Clinical	ENSP00000503633.1:p.Asp557Glu
ENST00000347559.6:c.1608+484T>G	ENSP00000292304.3:n.1608+484T>G
ENST00000361308.8:c.1416T>G	ENSP00000355292.5:p.Asp472Glu
ENST00000368297.5:c.1428T>G	ENSP00000357280.1:p.Asp476Glu
ENST00000368299.7:c.1671T>G	ENSP00000357282.3:p.Asp557Glu
ENST00000368300.8:c.1671T>G	ENSP00000357283.4:p.Asp557Glu
ENST00000368301.6:c.1671T>G	ENSP00000357284.2:p.Asp557Glu
ENST00000448611.6:c.1335T>G	ENSP00000395597.2:p.Asp445Glu
ENST00000473598.6:c.1374T>G	ENSP00000421821.1:p.Asp458Glu
ENST00000496738.5:n.1140T>G
ENST00000498722.2:n.903T>G
ENST00000506981.1:n.255T>G
ENST00000508500.1:c.486+484T>G	ENSP00000424977.1:n.486+484T>G
NM_001257374.2:c.1335T>G	NP_001244303.1:p.Asp445Glu
NM_001282624.1:c.1428T>G	NP_001269553.1:p.Asp476Glu
NM_001282625.1:c.1671T>G	NP_001269554.1:p.Asp557Glu
NM_001282626.1:c.1671T>G	NP_001269555.1:p.Asp557Glu
NM_005572.3:c.1671T>G , LRG_254t1:c.1671T>G	NP_005563.1:p.Asp557Glu
NM_170707.3:c.1671T>G	NP_733821.1:p.Asp557Glu
NM_170708.3:c.1608+484T>G	NP_733822.1:n.1608+484T>G
XM_011509533.1:c.1335T>G	XP_011507835.1:p.Asp445Glu
XM_011509534.1:c.1047T>G	XP_011507836.1:p.Asp349Glu
XR_921781.1:n.1960T>G
XM_011509534.2:c.1047T>G	XP_011507836.1:p.Asp349Glu
XR_921781.2:n.1958T>G
NM_170707.4:c.1671T>G MANE Select	NP_733821.1:p.Asp557Glu
NM_001257374.3:c.1335T>G	NP_001244303.1:p.Asp445Glu
NM_001282626.2:c.1671T>G	NP_001269555.1:p.Asp557Glu
NM_001282624.2:c.1428T>G	NP_001269553.1:p.Asp476Glu
NM_001282625.2:c.1671T>G	NP_001269554.1:p.Asp557Glu
NM_005572.4:c.1671T>G MANE Plus Clinical	NP_005563.1:p.Asp557Glu
NM_170708.4:c.1608+484T>G	NP_733822.1:n.1608+484T>G