Canonical Allele Identifier: CA2294855876

Gene: ASXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33739224_33739225delinsGC , CM000680.2:g.33739224_33739225delinsGC	GRCh38
NC_000018.9:g.31319188_31319189delinsGC , CM000680.1:g.31319188_31319189delinsGC	GRCh37
NC_000018.8:g.29573186_29573187delinsGC	NCBI36
NG_055244.1:g.165648_165649delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.1823_1824delinsGC	ENSP00000513003.1:p.Cys608=
ENST00000269197.12:c.1820_1821delinsGC MANE Select	ENSP00000269197.4:p.Cys607=
ENST00000592288.6:c.*944_*945delinsGC	ENSP00000465053.1:n.*944_*945delinsGC
ENST00000592541.6:c.*1479_*1480delinsGC	ENSP00000466655.2:n.*1479_*1480delinsGC
ENST00000593195.6:c.2032_2033delinsGC	ENSP00000466073.1:n.2032_2033delinsGC
ENST00000642541.1:c.1652_1653delinsGC	ENSP00000493665.1:p.Cys551=
ENST00000681521.1:c.1700_1701delinsGC	ENSP00000506037.1:p.Cys567=
ENST00000269197.9:c.1820_1821delinsGC	ENSP00000269197.4:p.Cys607=
ENST00000592288.5:c.*944_*945delinsGC	ENSP00000465053.1:n.*944_*945delinsGC
NM_030632.1:c.1820_1821delinsGC	NP_085135.1:p.Cys607=
XM_005258356.1:c.1823_1824delinsGC	XP_005258413.1:p.Cys608=
XM_011526205.1:c.1796_1797delinsGC	XP_011524507.1:p.Cys599=
XM_011526206.1:c.1742_1743delinsGC	XP_011524508.1:p.Cys581=
XM_011526207.1:c.1742_1743delinsGC	XP_011524509.1:p.Cys581=
XM_011526208.1:c.1703_1704delinsGC	XP_011524510.1:p.Cys568=
XM_011526209.1:c.1652_1653delinsGC	XP_011524511.1:p.Cys551=
XM_011526210.1:c.1652_1653delinsGC	XP_011524512.1:p.Cys551=
XM_011526211.1:c.1652_1653delinsGC	XP_011524513.1:p.Cys551=
XM_011526212.1:c.1652_1653delinsGC	XP_011524514.1:p.Cys551=
XM_011526213.1:c.1652_1653delinsGC	XP_011524515.1:p.Cys551=
XM_011526214.1:c.1652_1653delinsGC	XP_011524516.1:p.Cys551=
NM_030632.2:c.1820_1821delinsGC	NP_085135.1:p.Cys607=
XM_011526205.2:c.1796_1797delinsGC	XP_011524507.1:p.Cys599=
XM_011526206.2:c.1742_1743delinsGC	XP_011524508.1:p.Cys581=
XM_011526213.2:c.1652_1653delinsGC	XP_011524515.1:p.Cys551=
XM_017026012.1:c.1742_1743delinsGC	XP_016881501.1:p.Cys581=
XM_017026013.1:c.1652_1653delinsGC	XP_016881502.1:p.Cys551=
XM_017026014.2:c.1652_1653delinsGC	XP_016881503.1:p.Cys551=
XM_024451269.1:c.1652_1653delinsGC	XP_024307037.1:p.Cys551=
NM_030632.3:c.1820_1821delinsGC MANE Select	NP_085135.1:p.Cys607=