Canonical Allele Identifier: CA2294855788

Gene: ASXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33739026_33739028delinsACT , CM000680.2:g.33739026_33739028delinsACT	GRCh38
NC_000018.9:g.31318990_31318992delinsACT , CM000680.1:g.31318990_31318992delinsACT	GRCh37
NC_000018.8:g.29572988_29572990delinsACT	NCBI36
NG_055244.1:g.165450_165452delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.1625_1627delinsACT	ENSP00000513003.1:p.Asp542=
ENST00000269197.12:c.1622_1624delinsACT MANE Select	ENSP00000269197.4:p.Asp541=
ENST00000592288.6:c.*746_*748delinsACT	ENSP00000465053.1:n.*746_*748delinsACT
ENST00000592541.6:c.*1281_*1283delinsACT	ENSP00000466655.2:n.*1281_*1283delinsACT
ENST00000593195.6:c.1834_1836delinsACT	ENSP00000466073.1:n.1834_1836delinsACT
ENST00000642541.1:c.1454_1456delinsACT	ENSP00000493665.1:p.Asp485=
ENST00000681521.1:c.1502_1504delinsACT	ENSP00000506037.1:p.Asp501=
ENST00000269197.9:c.1622_1624delinsACT	ENSP00000269197.4:p.Asp541=
ENST00000592288.5:c.*746_*748delinsACT	ENSP00000465053.1:n.*746_*748delinsACT
NM_030632.1:c.1622_1624delinsACT	NP_085135.1:p.Asp541=
XM_005258356.1:c.1625_1627delinsACT	XP_005258413.1:p.Asp542=
XM_011526205.1:c.1598_1600delinsACT	XP_011524507.1:p.Asp533=
XM_011526206.1:c.1544_1546delinsACT	XP_011524508.1:p.Asp515=
XM_011526207.1:c.1544_1546delinsACT	XP_011524509.1:p.Asp515=
XM_011526208.1:c.1505_1507delinsACT	XP_011524510.1:p.Asp502=
XM_011526209.1:c.1454_1456delinsACT	XP_011524511.1:p.Asp485=
XM_011526210.1:c.1454_1456delinsACT	XP_011524512.1:p.Asp485=
XM_011526211.1:c.1454_1456delinsACT	XP_011524513.1:p.Asp485=
XM_011526212.1:c.1454_1456delinsACT	XP_011524514.1:p.Asp485=
XM_011526213.1:c.1454_1456delinsACT	XP_011524515.1:p.Asp485=
XM_011526214.1:c.1454_1456delinsACT	XP_011524516.1:p.Asp485=
NM_030632.2:c.1622_1624delinsACT	NP_085135.1:p.Asp541=
XM_011526205.2:c.1598_1600delinsACT	XP_011524507.1:p.Asp533=
XM_011526206.2:c.1544_1546delinsACT	XP_011524508.1:p.Asp515=
XM_011526213.2:c.1454_1456delinsACT	XP_011524515.1:p.Asp485=
XM_017026012.1:c.1544_1546delinsACT	XP_016881501.1:p.Asp515=
XM_017026013.1:c.1454_1456delinsACT	XP_016881502.1:p.Asp485=
XM_017026014.2:c.1454_1456delinsACT	XP_016881503.1:p.Asp485=
XM_024451269.1:c.1454_1456delinsACT	XP_024307037.1:p.Asp485=
NM_030632.3:c.1622_1624delinsACT MANE Select	NP_085135.1:p.Asp541=