Canonical Allele Identifier: CA1200473412

Gene: LMNA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156138395_156138396delinsCG , CM000663.2:g.156138395_156138396delinsCG	GRCh38
NC_000001.10:g.156108186_156108187delinsCG , CM000663.1:g.156108186_156108187delinsCG	GRCh37
NC_000001.9:g.154374810_154374811delinsCG	NCBI36
NG_008692.2:g.60823_60824delinsCG , LRG_254:g.60823_60824delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.1141-93_1141-92delinsCG	ENSP00000426535.3:n.1141-93_1141-92delinsCG
ENST00000682650.1:c.1609-93_1609-92delinsCG	ENSP00000506904.1:n.1609-93_1609-92delinsCG
ENST00000683032.1:c.1699-93_1699-92delinsCG	ENSP00000506771.1:n.1699-93_1699-92delinsCG
ENST00000683773.1:n.44-93_44-92delinsCG
ENST00000684195.1:c.*698_*699delinsCG	ENSP00000508220.1:n.*698_*699delinsCG
ENST00000361308.9:c.1699-93_1699-92delinsCG	ENSP00000355292.6:n.1699-93_1699-92delinsCG
ENST00000368300.9:c.1699-93_1699-92delinsCG MANE Select	ENSP00000357283.4:n.1699-93_1699-92delinsCG
ENST00000496738.6:n.2809_2810delinsCG
ENST00000674518.1:c.*1049-93_*1049-92delinsCG	ENSP00000502261.1:n.*1049-93_*1049-92delinsCG
ENST00000674600.1:c.*1498-93_*1498-92delinsCG	ENSP00000501666.1:n.*1498-93_*1498-92delinsCG
ENST00000674720.1:c.*912_*913delinsCG	ENSP00000502798.1:n.*912_*913delinsCG
ENST00000675455.1:c.*1499-93_*1499-92delinsCG	ENSP00000501795.1:n.*1499-93_*1499-92delinsCG
ENST00000675667.1:c.1699-93_1699-92delinsCG	ENSP00000501803.1:n.1699-93_1699-92delinsCG
ENST00000675874.1:c.*1170-93_*1170-92delinsCG	ENSP00000501851.1:n.*1170-93_*1170-92delinsCG
ENST00000675881.1:c.*710-93_*710-92delinsCG	ENSP00000501670.1:n.*710-93_*710-92delinsCG
ENST00000675939.1:c.1699-93_1699-92delinsCG	ENSP00000502256.1:n.1699-93_1699-92delinsCG
ENST00000675989.1:n.3209_3210delinsCG
ENST00000676208.1:c.*802-93_*802-92delinsCG	ENSP00000502468.1:n.*802-93_*802-92delinsCG
ENST00000676283.1:n.3146_3147delinsCG
ENST00000676385.2:c.1609-93_1609-92delinsCG	ENSP00000502091.1:n.1609-93_1609-92delinsCG
ENST00000676434.1:c.*1361_*1362delinsCG	ENSP00000501648.1:n.*1361_*1362delinsCG
ENST00000347559.6:c.1609-93_1609-92delinsCG	ENSP00000292304.3:n.1609-93_1609-92delinsCG
ENST00000368299.7:c.1699-93_1699-92delinsCG	ENSP00000357282.3:n.1699-93_1699-92delinsCG
ENST00000368300.8:c.1699-93_1699-92delinsCG	ENSP00000357283.4:n.1699-93_1699-92delinsCG
ENST00000448611.6:c.1363-93_1363-92delinsCG	ENSP00000395597.2:n.1363-93_1363-92delinsCG
ENST00000473598.6:c.1402-93_1402-92delinsCG	ENSP00000421821.1:n.1402-93_1402-92delinsCG
ENST00000496738.5:n.1819_1820delinsCG
ENST00000506981.1:n.283-93_283-92delinsCG
ENST00000508500.1:c.487-93_487-92delinsCG	ENSP00000424977.1:n.487-93_487-92delinsCG
NM_001257374.2:c.1363-93_1363-92delinsCG	NP_001244303.1:n.1363-93_1363-92delinsCG
NM_001282626.1:c.1699-93_1699-92delinsCG	NP_001269555.1:n.1699-93_1699-92delinsCG
NM_170707.3:c.1699-93_1699-92delinsCG	NP_733821.1:n.1699-93_1699-92delinsCG
NM_170708.3:c.1609-93_1609-92delinsCG	NP_733822.1:n.1609-93_1609-92delinsCG
XM_011509533.1:c.1363-93_1363-92delinsCG	XP_011507835.1:n.1363-93_1363-92delinsCG
XM_011509534.1:c.1075-93_1075-92delinsCG	XP_011507836.1:n.1075-93_1075-92delinsCG
XR_921781.1:n.1988-93_1988-92delinsCG
XM_011509534.2:c.1075-93_1075-92delinsCG	XP_011507836.1:n.1075-93_1075-92delinsCG
XR_921781.2:n.1986-93_1986-92delinsCG
NM_170707.4:c.1699-93_1699-92delinsCG MANE Select	NP_733821.1:n.1699-93_1699-92delinsCG
NM_001257374.3:c.1363-93_1363-92delinsCG	NP_001244303.1:n.1363-93_1363-92delinsCG
NM_001282626.2:c.1699-93_1699-92delinsCG	NP_001269555.1:n.1699-93_1699-92delinsCG
NM_170708.4:c.1609-93_1609-92delinsCG	NP_733822.1:n.1609-93_1609-92delinsCG