Canonical Allele Identifier: CA2648353394

Gene: LMNA

Linked Data

• gnomAD v4: 1-156138417-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156138419del , CM000663.2:g.156138419del	GRCh38
NC_000001.10:g.156108210del , CM000663.1:g.156108210del	GRCh37
NC_000001.9:g.154374834del	NCBI36
NG_008692.2:g.60847del , LRG_254:g.60847del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.1141-69del	ENSP00000426535.3:n.1141-69del
ENST00000682650.1:c.1609-69del	ENSP00000506904.1:n.1609-69del
ENST00000683032.1:c.1699-69del	ENSP00000506771.1:n.1699-69del
ENST00000683773.1:n.44-69del
ENST00000684195.1:c.*722del	ENSP00000508220.1:n.*722del
ENST00000361308.9:c.1699-69del	ENSP00000355292.6:n.1699-69del
ENST00000368300.9:c.1699-69del MANE Select	ENSP00000357283.4:n.1699-69del
ENST00000496738.6:n.2833del
ENST00000674518.1:c.*1049-69del	ENSP00000502261.1:n.*1049-69del
ENST00000674600.1:c.*1498-69del	ENSP00000501666.1:n.*1498-69del
ENST00000674720.1:c.*936del	ENSP00000502798.1:n.*936del
ENST00000675455.1:c.*1499-69del	ENSP00000501795.1:n.*1499-69del
ENST00000675667.1:c.1699-69del	ENSP00000501803.1:n.1699-69del
ENST00000675874.1:c.*1170-69del	ENSP00000501851.1:n.*1170-69del
ENST00000675881.1:c.*710-69del	ENSP00000501670.1:n.*710-69del
ENST00000675939.1:c.1699-69del	ENSP00000502256.1:n.1699-69del
ENST00000675989.1:n.3233del
ENST00000676208.1:c.*802-69del	ENSP00000502468.1:n.*802-69del
ENST00000676283.1:n.3170del
ENST00000676385.2:c.1609-69del	ENSP00000502091.1:n.1609-69del
ENST00000676434.1:c.*1385del	ENSP00000501648.1:n.*1385del
ENST00000347559.6:c.1609-69del	ENSP00000292304.3:n.1609-69del
ENST00000368299.7:c.1699-69del	ENSP00000357282.3:n.1699-69del
ENST00000368300.8:c.1699-69del	ENSP00000357283.4:n.1699-69del
ENST00000448611.6:c.1363-69del	ENSP00000395597.2:n.1363-69del
ENST00000473598.6:c.1402-69del	ENSP00000421821.1:n.1402-69del
ENST00000496738.5:n.1843del
ENST00000506981.1:n.283-69del
ENST00000508500.1:c.487-69del	ENSP00000424977.1:n.487-69del
NM_001257374.2:c.1363-69del	NP_001244303.1:n.1363-69del
NM_001282626.1:c.1699-69del	NP_001269555.1:n.1699-69del
NM_170707.3:c.1699-69del	NP_733821.1:n.1699-69del
NM_170708.3:c.1609-69del	NP_733822.1:n.1609-69del
XM_011509533.1:c.1363-69del	XP_011507835.1:n.1363-69del
XM_011509534.1:c.1075-69del	XP_011507836.1:n.1075-69del
XR_921781.1:n.1988-69del
XM_011509534.2:c.1075-69del	XP_011507836.1:n.1075-69del
XR_921781.2:n.1986-69del
NM_170707.4:c.1699-69del MANE Select	NP_733821.1:n.1699-69del
NM_001257374.3:c.1363-69del	NP_001244303.1:n.1363-69del
NM_001282626.2:c.1699-69del	NP_001269555.1:n.1699-69del
NM_170708.4:c.1609-69del	NP_733822.1:n.1609-69del