Canonical Allele Identifier: CA1008065519

Gene: LMNA

Linked Data

• gnomAD v3: 1-156136809-T-TCTC
• gnomAD v4: 1-156136809-T-TCTC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156136809_156136810insCTC , CM000663.2:g.156136809_156136810insCTC	GRCh38
NC_000001.10:g.156106600_156106601insCTC , CM000663.1:g.156106600_156106601insCTC	GRCh37
NC_000001.9:g.154373224_154373225insCTC	NCBI36
NG_008692.2:g.59237_59238insCTC , LRG_254:g.59237_59238insCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.823-112_823-111insCTC	ENSP00000426535.3:n.823-112_823-111insCTC
ENST00000459904.2:n.517_518insCTC
ENST00000498722.3:n.613-112_613-111insCTC
ENST00000682650.1:c.1381-112_1381-111insCTC	ENSP00000506904.1:n.1381-112_1381-111insCTC
ENST00000683032.1:c.1381-112_1381-111insCTC	ENSP00000506771.1:n.1381-112_1381-111insCTC
ENST00000684195.1:c.1381-112_1381-111insCTC	ENSP00000508220.1:n.1381-112_1381-111insCTC
ENST00000361308.9:c.1381-112_1381-111insCTC	ENSP00000355292.6:n.1381-112_1381-111insCTC
ENST00000368300.9:c.1381-112_1381-111insCTC MANE Select	ENSP00000357283.4:n.1381-112_1381-111insCTC
ENST00000496738.6:n.1756-112_1756-111insCTC
ENST00000674518.1:c.*731-112_*731-111insCTC	ENSP00000502261.1:n.*731-112_*731-111insCTC
ENST00000674600.1:c.*1180-112_*1180-111insCTC	ENSP00000501666.1:n.*1180-112_*1180-111insCTC
ENST00000674720.1:c.1494-112_1494-111insCTC	ENSP00000502798.1:n.1494-112_1494-111insCTC
ENST00000675431.1:n.1074-112_1074-111insCTC
ENST00000675455.1:c.*1181-112_*1181-111insCTC	ENSP00000501795.1:n.*1181-112_*1181-111insCTC
ENST00000675667.1:c.1381-112_1381-111insCTC	ENSP00000501803.1:n.1381-112_1381-111insCTC
ENST00000675874.1:c.*852-112_*852-111insCTC	ENSP00000501851.1:n.*852-112_*852-111insCTC
ENST00000675881.1:c.*392-112_*392-111insCTC	ENSP00000501670.1:n.*392-112_*392-111insCTC
ENST00000675939.1:c.1381-112_1381-111insCTC	ENSP00000502256.1:n.1381-112_1381-111insCTC
ENST00000675989.1:n.2128_2129insCTC
ENST00000676208.1:c.*484-112_*484-111insCTC	ENSP00000502468.1:n.*484-112_*484-111insCTC
ENST00000676283.1:n.1756-112_1756-111insCTC
ENST00000676385.2:c.1381-112_1381-111insCTC	ENSP00000502091.1:n.1381-112_1381-111insCTC
ENST00000676434.1:c.*392-112_*392-111insCTC	ENSP00000501648.1:n.*392-112_*392-111insCTC
ENST00000677389.1:c.1381-112_1381-111insCTC MANE Plus Clinical	ENSP00000503633.1:n.1381-112_1381-111insCTC
ENST00000347559.6:c.1381-112_1381-111insCTC	ENSP00000292304.3:n.1381-112_1381-111insCTC
ENST00000361308.8:c.1312-382_1312-381insCTC	ENSP00000355292.5:n.1312-382_1312-381insCTC
ENST00000368297.5:c.1138-112_1138-111insCTC	ENSP00000357280.1:n.1138-112_1138-111insCTC
ENST00000368298.2:n.1017_1018insCTC
ENST00000368299.7:c.1381-112_1381-111insCTC	ENSP00000357282.3:n.1381-112_1381-111insCTC
ENST00000368300.8:c.1381-112_1381-111insCTC	ENSP00000357283.4:n.1381-112_1381-111insCTC
ENST00000368301.6:c.1381-112_1381-111insCTC	ENSP00000357284.2:n.1381-112_1381-111insCTC
ENST00000448611.6:c.1045-112_1045-111insCTC	ENSP00000395597.2:n.1045-112_1045-111insCTC
ENST00000459904.1:n.517_518insCTC
ENST00000473598.6:c.1084-112_1084-111insCTC	ENSP00000421821.1:n.1084-112_1084-111insCTC
ENST00000496738.5:n.766-112_766-111insCTC
ENST00000498722.2:n.613-112_613-111insCTC
ENST00000508500.1:c.259-112_259-111insCTC	ENSP00000424977.1:n.259-112_259-111insCTC
NM_001257374.2:c.1045-112_1045-111insCTC	NP_001244303.1:n.1045-112_1045-111insCTC
NM_001282624.1:c.1138-112_1138-111insCTC	NP_001269553.1:n.1138-112_1138-111insCTC
NM_001282625.1:c.1381-112_1381-111insCTC	NP_001269554.1:n.1381-112_1381-111insCTC
NM_001282626.1:c.1381-112_1381-111insCTC	NP_001269555.1:n.1381-112_1381-111insCTC
NM_005572.3:c.1381-112_1381-111insCTC , LRG_254t1:c.1381-112_1381-111insCTC	NP_005563.1:n.1381-112_1381-111insCTC
NM_170707.3:c.1381-112_1381-111insCTC	NP_733821.1:n.1381-112_1381-111insCTC
NM_170708.3:c.1381-112_1381-111insCTC	NP_733822.1:n.1381-112_1381-111insCTC
XM_011509533.1:c.1045-112_1045-111insCTC	XP_011507835.1:n.1045-112_1045-111insCTC
XM_011509534.1:c.757-112_757-111insCTC	XP_011507836.1:n.757-112_757-111insCTC
XR_921781.1:n.1670-112_1670-111insCTC
XM_011509534.2:c.757-112_757-111insCTC	XP_011507836.1:n.757-112_757-111insCTC
XR_921781.2:n.1668-112_1668-111insCTC
NM_170707.4:c.1381-112_1381-111insCTC MANE Select	NP_733821.1:n.1381-112_1381-111insCTC
NM_001257374.3:c.1045-112_1045-111insCTC	NP_001244303.1:n.1045-112_1045-111insCTC
NM_001282626.2:c.1381-112_1381-111insCTC	NP_001269555.1:n.1381-112_1381-111insCTC
NM_001282624.2:c.1138-112_1138-111insCTC	NP_001269553.1:n.1138-112_1138-111insCTC
NM_001282625.2:c.1381-112_1381-111insCTC	NP_001269554.1:n.1381-112_1381-111insCTC
NM_005572.4:c.1381-112_1381-111insCTC MANE Plus Clinical	NP_005563.1:n.1381-112_1381-111insCTC
NM_170708.4:c.1381-112_1381-111insCTC	NP_733822.1:n.1381-112_1381-111insCTC