Canonical Allele Identifier: CA2648349575

Gene: LMNA

Linked Data

• gnomAD v4: 1-156136797-GGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156136804_156136805del , CM000663.2:g.156136804_156136805del	GRCh38
NC_000001.10:g.156106595_156106596del , CM000663.1:g.156106595_156106596del	GRCh37
NC_000001.9:g.154373219_154373220del	NCBI36
NG_008692.2:g.59232_59233del , LRG_254:g.59232_59233del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.823-117_823-116del	ENSP00000426535.3:n.823-117_823-116del
ENST00000459904.2:n.512_513del
ENST00000498722.3:n.613-117_613-116del
ENST00000682650.1:c.1381-117_1381-116del	ENSP00000506904.1:n.1381-117_1381-116del
ENST00000683032.1:c.1381-117_1381-116del	ENSP00000506771.1:n.1381-117_1381-116del
ENST00000684195.1:c.1381-117_1381-116del	ENSP00000508220.1:n.1381-117_1381-116del
ENST00000361308.9:c.1381-117_1381-116del	ENSP00000355292.6:n.1381-117_1381-116del
ENST00000368300.9:c.1381-117_1381-116del MANE Select	ENSP00000357283.4:n.1381-117_1381-116del
ENST00000496738.6:n.1756-117_1756-116del
ENST00000674518.1:c.*731-117_*731-116del	ENSP00000502261.1:n.*731-117_*731-116del
ENST00000674600.1:c.*1180-117_*1180-116del	ENSP00000501666.1:n.*1180-117_*1180-116del
ENST00000674720.1:c.1494-117_1494-116del	ENSP00000502798.1:n.1494-117_1494-116del
ENST00000675431.1:n.1074-117_1074-116del
ENST00000675455.1:c.*1181-117_*1181-116del	ENSP00000501795.1:n.*1181-117_*1181-116del
ENST00000675667.1:c.1381-117_1381-116del	ENSP00000501803.1:n.1381-117_1381-116del
ENST00000675874.1:c.*852-117_*852-116del	ENSP00000501851.1:n.*852-117_*852-116del
ENST00000675881.1:c.*392-117_*392-116del	ENSP00000501670.1:n.*392-117_*392-116del
ENST00000675939.1:c.1381-117_1381-116del	ENSP00000502256.1:n.1381-117_1381-116del
ENST00000675989.1:n.2123_2124del
ENST00000676208.1:c.*484-117_*484-116del	ENSP00000502468.1:n.*484-117_*484-116del
ENST00000676283.1:n.1756-117_1756-116del
ENST00000676385.2:c.1381-117_1381-116del	ENSP00000502091.1:n.1381-117_1381-116del
ENST00000676434.1:c.*392-117_*392-116del	ENSP00000501648.1:n.*392-117_*392-116del
ENST00000677389.1:c.1381-117_1381-116del MANE Plus Clinical	ENSP00000503633.1:n.1381-117_1381-116del
ENST00000347559.6:c.1381-117_1381-116del	ENSP00000292304.3:n.1381-117_1381-116del
ENST00000361308.8:c.1312-387_1312-386del	ENSP00000355292.5:n.1312-387_1312-386del
ENST00000368297.5:c.1138-117_1138-116del	ENSP00000357280.1:n.1138-117_1138-116del
ENST00000368298.2:n.1012_1013del
ENST00000368299.7:c.1381-117_1381-116del	ENSP00000357282.3:n.1381-117_1381-116del
ENST00000368300.8:c.1381-117_1381-116del	ENSP00000357283.4:n.1381-117_1381-116del
ENST00000368301.6:c.1381-117_1381-116del	ENSP00000357284.2:n.1381-117_1381-116del
ENST00000448611.6:c.1045-117_1045-116del	ENSP00000395597.2:n.1045-117_1045-116del
ENST00000459904.1:n.512_513del
ENST00000473598.6:c.1084-117_1084-116del	ENSP00000421821.1:n.1084-117_1084-116del
ENST00000496738.5:n.766-117_766-116del
ENST00000498722.2:n.613-117_613-116del
ENST00000508500.1:c.259-117_259-116del	ENSP00000424977.1:n.259-117_259-116del
NM_001257374.2:c.1045-117_1045-116del	NP_001244303.1:n.1045-117_1045-116del
NM_001282624.1:c.1138-117_1138-116del	NP_001269553.1:n.1138-117_1138-116del
NM_001282625.1:c.1381-117_1381-116del	NP_001269554.1:n.1381-117_1381-116del
NM_001282626.1:c.1381-117_1381-116del	NP_001269555.1:n.1381-117_1381-116del
NM_005572.3:c.1381-117_1381-116del , LRG_254t1:c.1381-117_1381-116del	NP_005563.1:n.1381-117_1381-116del
NM_170707.3:c.1381-117_1381-116del	NP_733821.1:n.1381-117_1381-116del
NM_170708.3:c.1381-117_1381-116del	NP_733822.1:n.1381-117_1381-116del
XM_011509533.1:c.1045-117_1045-116del	XP_011507835.1:n.1045-117_1045-116del
XM_011509534.1:c.757-117_757-116del	XP_011507836.1:n.757-117_757-116del
XR_921781.1:n.1670-117_1670-116del
XM_011509534.2:c.757-117_757-116del	XP_011507836.1:n.757-117_757-116del
XR_921781.2:n.1668-117_1668-116del
NM_170707.4:c.1381-117_1381-116del MANE Select	NP_733821.1:n.1381-117_1381-116del
NM_001257374.3:c.1045-117_1045-116del	NP_001244303.1:n.1045-117_1045-116del
NM_001282626.2:c.1381-117_1381-116del	NP_001269555.1:n.1381-117_1381-116del
NM_001282624.2:c.1138-117_1138-116del	NP_001269553.1:n.1138-117_1138-116del
NM_001282625.2:c.1381-117_1381-116del	NP_001269554.1:n.1381-117_1381-116del
NM_005572.4:c.1381-117_1381-116del MANE Plus Clinical	NP_005563.1:n.1381-117_1381-116del
NM_170708.4:c.1381-117_1381-116del	NP_733822.1:n.1381-117_1381-116del