Canonical Allele Identifier: CA2294854272

Gene: ASXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33735799_33735804delinsATTAAT , CM000680.2:g.33735799_33735804delinsATTAAT	GRCh38
NC_000018.9:g.31315763_31315768delinsATTAAT , CM000680.1:g.31315763_31315768delinsATTAAT	GRCh37
NC_000018.8:g.29569761_29569766delinsATTAAT	NCBI36
NG_055244.1:g.162223_162228delinsATTAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.1085+1384_1085+1389delinsATTAAT	ENSP00000513003.1:n.1085+1384_1085+1389delinsATTAAT
ENST00000269197.12:c.1082+1384_1082+1389delinsATTAAT MANE Select	ENSP00000269197.4:n.1082+1384_1082+1389delinsATTAAT
ENST00000592288.6:c.*206+1384_*206+1389delinsATTAAT	ENSP00000465053.1:n.*206+1384_*206+1389delinsATTAAT
ENST00000592541.6:c.*741+1384_*741+1389delinsATTAAT	ENSP00000466655.2:n.*741+1384_*741+1389delinsATTAAT
ENST00000593195.6:c.1294+1384_1294+1389delinsATTAAT	ENSP00000466073.1:n.1294+1384_1294+1389delinsATTAAT
ENST00000642541.1:c.914+1384_914+1389delinsATTAAT	ENSP00000493665.1:n.914+1384_914+1389delinsATTAAT
ENST00000681521.1:c.962+1384_962+1389delinsATTAAT	ENSP00000506037.1:n.962+1384_962+1389delinsATTAAT
ENST00000269197.9:c.1082+1384_1082+1389delinsATTAAT	ENSP00000269197.4:n.1082+1384_1082+1389delinsATTAAT
ENST00000592288.5:c.*206+1384_*206+1389delinsATTAAT	ENSP00000465053.1:n.*206+1384_*206+1389delinsATTAAT
NM_030632.1:c.1082+1384_1082+1389delinsATTAAT	NP_085135.1:n.1082+1384_1082+1389delinsATTAAT
XM_005258356.1:c.1085+1384_1085+1389delinsATTAAT	XP_005258413.1:n.1085+1384_1085+1389delinsATTAAT
XM_011526205.1:c.1058+1384_1058+1389delinsATTAAT	XP_011524507.1:n.1058+1384_1058+1389delinsATTAAT
XM_011526206.1:c.1004+1384_1004+1389delinsATTAAT	XP_011524508.1:n.1004+1384_1004+1389delinsATTAAT
XM_011526207.1:c.1004+1384_1004+1389delinsATTAAT	XP_011524509.1:n.1004+1384_1004+1389delinsATTAAT
XM_011526208.1:c.965+1384_965+1389delinsATTAAT	XP_011524510.1:n.965+1384_965+1389delinsATTAAT
XM_011526209.1:c.914+1384_914+1389delinsATTAAT	XP_011524511.1:n.914+1384_914+1389delinsATTAAT
XM_011526210.1:c.914+1384_914+1389delinsATTAAT	XP_011524512.1:n.914+1384_914+1389delinsATTAAT
XM_011526211.1:c.914+1384_914+1389delinsATTAAT	XP_011524513.1:n.914+1384_914+1389delinsATTAAT
XM_011526212.1:c.914+1384_914+1389delinsATTAAT	XP_011524514.1:n.914+1384_914+1389delinsATTAAT
XM_011526213.1:c.914+1384_914+1389delinsATTAAT	XP_011524515.1:n.914+1384_914+1389delinsATTAAT
XM_011526214.1:c.914+1384_914+1389delinsATTAAT	XP_011524516.1:n.914+1384_914+1389delinsATTAAT
NM_030632.2:c.1082+1384_1082+1389delinsATTAAT	NP_085135.1:n.1082+1384_1082+1389delinsATTAAT
XM_011526205.2:c.1058+1384_1058+1389delinsATTAAT	XP_011524507.1:n.1058+1384_1058+1389delinsATTAAT
XM_011526206.2:c.1004+1384_1004+1389delinsATTAAT	XP_011524508.1:n.1004+1384_1004+1389delinsATTAAT
XM_011526213.2:c.914+1384_914+1389delinsATTAAT	XP_011524515.1:n.914+1384_914+1389delinsATTAAT
XM_017026012.1:c.1004+1384_1004+1389delinsATTAAT	XP_016881501.1:n.1004+1384_1004+1389delinsATTAAT
XM_017026013.1:c.914+1384_914+1389delinsATTAAT	XP_016881502.1:n.914+1384_914+1389delinsATTAAT
XM_017026014.2:c.914+1384_914+1389delinsATTAAT	XP_016881503.1:n.914+1384_914+1389delinsATTAAT
XM_024451269.1:c.914+1384_914+1389delinsATTAAT	XP_024307037.1:n.914+1384_914+1389delinsATTAAT
NM_030632.3:c.1082+1384_1082+1389delinsATTAAT MANE Select	NP_085135.1:n.1082+1384_1082+1389delinsATTAAT