Canonical Allele Identifier: CA1200473401

Gene: LMNA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156138373_156138374delinsAG , CM000663.2:g.156138373_156138374delinsAG	GRCh38
NC_000001.10:g.156108164_156108165delinsAG , CM000663.1:g.156108164_156108165delinsAG	GRCh37
NC_000001.9:g.154374788_154374789delinsAG	NCBI36
NG_008692.2:g.60801_60802delinsAG , LRG_254:g.60801_60802delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.1141-115_1141-114delinsAG	ENSP00000426535.3:n.1141-115_1141-114delinsAG
ENST00000682650.1:c.1609-115_1609-114delinsAG	ENSP00000506904.1:n.1609-115_1609-114delinsAG
ENST00000683032.1:c.1699-115_1699-114delinsAG	ENSP00000506771.1:n.1699-115_1699-114delinsAG
ENST00000683773.1:n.44-115_44-114delinsAG
ENST00000684195.1:c.*676_*677delinsAG	ENSP00000508220.1:n.*676_*677delinsAG
ENST00000361308.9:c.1699-115_1699-114delinsAG	ENSP00000355292.6:n.1699-115_1699-114delinsAG
ENST00000368300.9:c.1699-115_1699-114delinsAG MANE Select	ENSP00000357283.4:n.1699-115_1699-114delinsAG
ENST00000496738.6:n.2787_2788delinsAG
ENST00000674518.1:c.*1049-115_*1049-114delinsAG	ENSP00000502261.1:n.*1049-115_*1049-114delinsAG
ENST00000674600.1:c.*1498-115_*1498-114delinsAG	ENSP00000501666.1:n.*1498-115_*1498-114delinsAG
ENST00000674720.1:c.*890_*891delinsAG	ENSP00000502798.1:n.*890_*891delinsAG
ENST00000675455.1:c.*1499-115_*1499-114delinsAG	ENSP00000501795.1:n.*1499-115_*1499-114delinsAG
ENST00000675667.1:c.1699-115_1699-114delinsAG	ENSP00000501803.1:n.1699-115_1699-114delinsAG
ENST00000675874.1:c.*1170-115_*1170-114delinsAG	ENSP00000501851.1:n.*1170-115_*1170-114delinsAG
ENST00000675881.1:c.*710-115_*710-114delinsAG	ENSP00000501670.1:n.*710-115_*710-114delinsAG
ENST00000675939.1:c.1699-115_1699-114delinsAG	ENSP00000502256.1:n.1699-115_1699-114delinsAG
ENST00000675989.1:n.3187_3188delinsAG
ENST00000676208.1:c.*802-115_*802-114delinsAG	ENSP00000502468.1:n.*802-115_*802-114delinsAG
ENST00000676283.1:n.3124_3125delinsAG
ENST00000676385.2:c.1609-115_1609-114delinsAG	ENSP00000502091.1:n.1609-115_1609-114delinsAG
ENST00000676434.1:c.*1339_*1340delinsAG	ENSP00000501648.1:n.*1339_*1340delinsAG
ENST00000347559.6:c.1609-115_1609-114delinsAG	ENSP00000292304.3:n.1609-115_1609-114delinsAG
ENST00000368299.7:c.1699-115_1699-114delinsAG	ENSP00000357282.3:n.1699-115_1699-114delinsAG
ENST00000368300.8:c.1699-115_1699-114delinsAG	ENSP00000357283.4:n.1699-115_1699-114delinsAG
ENST00000448611.6:c.1363-115_1363-114delinsAG	ENSP00000395597.2:n.1363-115_1363-114delinsAG
ENST00000473598.6:c.1402-115_1402-114delinsAG	ENSP00000421821.1:n.1402-115_1402-114delinsAG
ENST00000496738.5:n.1797_1798delinsAG
ENST00000506981.1:n.283-115_283-114delinsAG
ENST00000508500.1:c.487-115_487-114delinsAG	ENSP00000424977.1:n.487-115_487-114delinsAG
NM_001257374.2:c.1363-115_1363-114delinsAG	NP_001244303.1:n.1363-115_1363-114delinsAG
NM_001282626.1:c.1699-115_1699-114delinsAG	NP_001269555.1:n.1699-115_1699-114delinsAG
NM_170707.3:c.1699-115_1699-114delinsAG	NP_733821.1:n.1699-115_1699-114delinsAG
NM_170708.3:c.1609-115_1609-114delinsAG	NP_733822.1:n.1609-115_1609-114delinsAG
XM_011509533.1:c.1363-115_1363-114delinsAG	XP_011507835.1:n.1363-115_1363-114delinsAG
XM_011509534.1:c.1075-115_1075-114delinsAG	XP_011507836.1:n.1075-115_1075-114delinsAG
XR_921781.1:n.1988-115_1988-114delinsAG
XM_011509534.2:c.1075-115_1075-114delinsAG	XP_011507836.1:n.1075-115_1075-114delinsAG
XR_921781.2:n.1986-115_1986-114delinsAG
NM_170707.4:c.1699-115_1699-114delinsAG MANE Select	NP_733821.1:n.1699-115_1699-114delinsAG
NM_001257374.3:c.1363-115_1363-114delinsAG	NP_001244303.1:n.1363-115_1363-114delinsAG
NM_001282626.2:c.1699-115_1699-114delinsAG	NP_001269555.1:n.1699-115_1699-114delinsAG
NM_170708.4:c.1609-115_1609-114delinsAG	NP_733822.1:n.1609-115_1609-114delinsAG