Canonical Allele Identifier: CA2294857605

Gene: ASXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33743212C= , CM000680.2:g.33743212C=	GRCh38
NC_000018.9:g.31323176C= , CM000680.1:g.31323176C=	GRCh37
NC_000018.8:g.29577174C=	NCBI36
NG_055244.1:g.169636C=

Transcript Alleles

HGVS	Amino-acid Change
NM_030632.3:c.3364C= MANE Select	NP_085135.1:p.Gln1122=
ENST00000269197.12:c.3364C= MANE Select	ENSP00000269197.4:p.Gln1122=
NM_030632.1:c.3364C=	NP_085135.1:p.Gln1122=
NM_030632.2:c.3364C=	NP_085135.1:p.Gln1122=
ENST00000269197.9:c.3364C=	ENSP00000269197.4:p.Gln1122=
ENST00000592288.5:c.*2488C=	ENSP00000465053.1:n.*2488C=
ENST00000592288.6:c.*2488C=	ENSP00000465053.1:n.*2488C=
ENST00000592541.6:c.*3023C=	ENSP00000466655.2:n.*3023C=
ENST00000593195.6:c.3576C=	ENSP00000466073.1:n.3576C=
ENST00000642541.1:c.3196C=	ENSP00000493665.1:p.Gln1066=
ENST00000681521.1:c.3244C=	ENSP00000506037.1:p.Gln1082=
ENST00000696964.1:c.3367C=	ENSP00000513003.1:p.Gln1123=
XM_005258356.1:c.3367C=	XP_005258413.1:p.Gln1123=
XM_011526205.1:c.3340C=	XP_011524507.1:p.Gln1114=
XM_011526205.2:c.3340C=	XP_011524507.1:p.Gln1114=
XM_011526206.1:c.3286C=	XP_011524508.1:p.Gln1096=
XM_011526206.2:c.3286C=	XP_011524508.1:p.Gln1096=
XM_011526207.1:c.3286C=	XP_011524509.1:p.Gln1096=
XM_011526208.1:c.3247C=	XP_011524510.1:p.Gln1083=
XM_011526209.1:c.3196C=	XP_011524511.1:p.Gln1066=
XM_011526210.1:c.3196C=	XP_011524512.1:p.Gln1066=
XM_011526211.1:c.3196C=	XP_011524513.1:p.Gln1066=
XM_011526212.1:c.3196C=	XP_011524514.1:p.Gln1066=
XM_011526213.1:c.3196C=	XP_011524515.1:p.Gln1066=
XM_011526213.2:c.3196C=	XP_011524515.1:p.Gln1066=
XM_011526214.1:c.3196C=	XP_011524516.1:p.Gln1066=
XM_011526215.1:c.328C=	XP_011524517.1:p.Gln110=
XM_017026012.1:c.3286C=	XP_016881501.1:p.Gln1096=
XM_017026013.1:c.3196C=	XP_016881502.1:p.Gln1066=
XM_017026014.2:c.3196C=	XP_016881503.1:p.Gln1066=
XM_024451269.1:c.3196C=	XP_024307037.1:p.Gln1066=