Canonical Allele Identifier: CA2294855749

Gene: ASXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33738936_33738938delinsCTT , CM000680.2:g.33738936_33738938delinsCTT	GRCh38
NC_000018.9:g.31318900_31318902delinsCTT , CM000680.1:g.31318900_31318902delinsCTT	GRCh37
NC_000018.8:g.29572898_29572900delinsCTT	NCBI36
NG_055244.1:g.165360_165362delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.1535_1537delinsCTT	ENSP00000513003.1:p.Thr512=
ENST00000269197.12:c.1532_1534delinsCTT MANE Select	ENSP00000269197.4:p.Thr511=
ENST00000592288.6:c.*656_*658delinsCTT	ENSP00000465053.1:n.*656_*658delinsCTT
ENST00000592541.6:c.*1191_*1193delinsCTT	ENSP00000466655.2:n.*1191_*1193delinsCTT
ENST00000593195.6:c.1744_1746delinsCTT	ENSP00000466073.1:n.1744_1746delinsCTT
ENST00000642541.1:c.1364_1366delinsCTT	ENSP00000493665.1:p.Thr455=
ENST00000681521.1:c.1412_1414delinsCTT	ENSP00000506037.1:p.Thr471=
ENST00000269197.9:c.1532_1534delinsCTT	ENSP00000269197.4:p.Thr511=
ENST00000592288.5:c.*656_*658delinsCTT	ENSP00000465053.1:n.*656_*658delinsCTT
NM_030632.1:c.1532_1534delinsCTT	NP_085135.1:p.Thr511=
XM_005258356.1:c.1535_1537delinsCTT	XP_005258413.1:p.Thr512=
XM_011526205.1:c.1508_1510delinsCTT	XP_011524507.1:p.Thr503=
XM_011526206.1:c.1454_1456delinsCTT	XP_011524508.1:p.Thr485=
XM_011526207.1:c.1454_1456delinsCTT	XP_011524509.1:p.Thr485=
XM_011526208.1:c.1415_1417delinsCTT	XP_011524510.1:p.Thr472=
XM_011526209.1:c.1364_1366delinsCTT	XP_011524511.1:p.Thr455=
XM_011526210.1:c.1364_1366delinsCTT	XP_011524512.1:p.Thr455=
XM_011526211.1:c.1364_1366delinsCTT	XP_011524513.1:p.Thr455=
XM_011526212.1:c.1364_1366delinsCTT	XP_011524514.1:p.Thr455=
XM_011526213.1:c.1364_1366delinsCTT	XP_011524515.1:p.Thr455=
XM_011526214.1:c.1364_1366delinsCTT	XP_011524516.1:p.Thr455=
NM_030632.2:c.1532_1534delinsCTT	NP_085135.1:p.Thr511=
XM_011526205.2:c.1508_1510delinsCTT	XP_011524507.1:p.Thr503=
XM_011526206.2:c.1454_1456delinsCTT	XP_011524508.1:p.Thr485=
XM_011526213.2:c.1364_1366delinsCTT	XP_011524515.1:p.Thr455=
XM_017026012.1:c.1454_1456delinsCTT	XP_016881501.1:p.Thr485=
XM_017026013.1:c.1364_1366delinsCTT	XP_016881502.1:p.Thr455=
XM_017026014.2:c.1364_1366delinsCTT	XP_016881503.1:p.Thr455=
XM_024451269.1:c.1364_1366delinsCTT	XP_024307037.1:p.Thr455=
NM_030632.3:c.1532_1534delinsCTT MANE Select	NP_085135.1:p.Thr511=