Canonical Allele Identifier: CA1143538358

Gene: LMNA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156136077_156136078delinsGG , CM000663.2:g.156136077_156136078delinsGG	GRCh38
NC_000001.10:g.156105868_156105869delinsGG , CM000663.1:g.156105868_156105869delinsGG	GRCh37
NC_000001.9:g.154372492_154372493delinsGG	NCBI36
NG_008692.2:g.58505_58506delinsGG , LRG_254:g.58505_58506delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.555_556delinsGG	ENSP00000426535.3:p.Met185=
ENST00000498722.3:n.345_346delinsGG
ENST00000682650.1:c.1113_1114delinsGG	ENSP00000506904.1:p.Met371=
ENST00000683032.1:c.1113_1114delinsGG	ENSP00000506771.1:p.Met371=
ENST00000684195.1:c.1113_1114delinsGG	ENSP00000508220.1:p.Met371=
ENST00000361308.9:c.1113_1114delinsGG	ENSP00000355292.6:p.Met371=
ENST00000368300.9:c.1113_1114delinsGG MANE Select	ENSP00000357283.4:p.Met371=
ENST00000496738.6:n.1488_1489delinsGG
ENST00000674518.1:c.*463_*464delinsGG	ENSP00000502261.1:n.*463_*464delinsGG
ENST00000674600.1:c.*912_*913delinsGG	ENSP00000501666.1:n.*912_*913delinsGG
ENST00000674720.1:c.1113_1114delinsGG	ENSP00000502798.1:p.Met371=
ENST00000675431.1:n.806_807delinsGG
ENST00000675455.1:c.*913_*914delinsGG	ENSP00000501795.1:n.*913_*914delinsGG
ENST00000675667.1:c.1113_1114delinsGG	ENSP00000501803.1:p.Met371=
ENST00000675874.1:c.*584_*585delinsGG	ENSP00000501851.1:n.*584_*585delinsGG
ENST00000675881.1:c.*124_*125delinsGG	ENSP00000501670.1:n.*124_*125delinsGG
ENST00000675939.1:c.1113_1114delinsGG	ENSP00000502256.1:p.Met371=
ENST00000675989.1:n.1488_1489delinsGG
ENST00000676208.1:c.*124_*125delinsGG	ENSP00000502468.1:n.*124_*125delinsGG
ENST00000676283.1:n.1488_1489delinsGG
ENST00000676385.2:c.1113_1114delinsGG	ENSP00000502091.1:p.Met371=
ENST00000676434.1:c.*124_*125delinsGG	ENSP00000501648.1:n.*124_*125delinsGG
ENST00000677389.1:c.1113_1114delinsGG MANE Plus Clinical	ENSP00000503633.1:p.Met371=
ENST00000347559.6:c.1113_1114delinsGG	ENSP00000292304.3:p.Met371=
ENST00000361308.8:c.1113_1114delinsGG	ENSP00000355292.5:p.Met371=
ENST00000368297.5:c.870_871delinsGG	ENSP00000357280.1:p.Met290=
ENST00000368298.2:n.377_378delinsGG
ENST00000368299.7:c.1113_1114delinsGG	ENSP00000357282.3:p.Met371=
ENST00000368300.8:c.1113_1114delinsGG	ENSP00000357283.4:p.Met371=
ENST00000368301.6:c.1113_1114delinsGG	ENSP00000357284.2:p.Met371=
ENST00000448611.6:c.777_778delinsGG	ENSP00000395597.2:p.Met259=
ENST00000473598.6:c.816_817delinsGG	ENSP00000421821.1:p.Met272=
ENST00000496738.5:n.498_499delinsGG
ENST00000498722.2:n.345_346delinsGG
NM_001257374.2:c.777_778delinsGG	NP_001244303.1:p.Met259=
NM_001282624.1:c.870_871delinsGG	NP_001269553.1:p.Met290=
NM_001282625.1:c.1113_1114delinsGG	NP_001269554.1:p.Met371=
NM_001282626.1:c.1113_1114delinsGG	NP_001269555.1:p.Met371=
NM_005572.3:c.1113_1114delinsGG , LRG_254t1:c.1113_1114delinsGG	NP_005563.1:p.Met371=
NM_170707.3:c.1113_1114delinsGG	NP_733821.1:p.Met371=
NM_170708.3:c.1113_1114delinsGG	NP_733822.1:p.Met371=
XM_011509533.1:c.777_778delinsGG	XP_011507835.1:p.Met259=
XM_011509534.1:c.489_490delinsGG	XP_011507836.1:p.Met163=
XR_921781.1:n.1402_1403delinsGG
XM_011509534.2:c.489_490delinsGG	XP_011507836.1:p.Met163=
XR_921781.2:n.1400_1401delinsGG
NM_170707.4:c.1113_1114delinsGG MANE Select	NP_733821.1:p.Met371=
NM_001257374.3:c.777_778delinsGG	NP_001244303.1:p.Met259=
NM_001282626.2:c.1113_1114delinsGG	NP_001269555.1:p.Met371=
NM_001282624.2:c.870_871delinsGG	NP_001269553.1:p.Met290=
NM_001282625.2:c.1113_1114delinsGG	NP_001269554.1:p.Met371=
NM_005572.4:c.1113_1114delinsGG MANE Plus Clinical	NP_005563.1:p.Met371=
NM_170708.4:c.1113_1114delinsGG	NP_733822.1:p.Met371=