Canonical Allele Identifier: CA2294855968

Gene: ASXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33739424G= , CM000680.2:g.33739424G=	GRCh38
NC_000018.9:g.31319388G= , CM000680.1:g.31319388G=	GRCh37
NC_000018.8:g.29573386G=	NCBI36
NG_055244.1:g.165848G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.2023G=	ENSP00000513003.1:p.Ala675=
ENST00000269197.12:c.2020G= MANE Select	ENSP00000269197.4:p.Ala674=
ENST00000592288.6:c.*1144G=	ENSP00000465053.1:n.*1144G=
ENST00000592541.6:c.*1679G=	ENSP00000466655.2:n.*1679G=
ENST00000593195.6:c.2232G=	ENSP00000466073.1:n.2232G=
ENST00000642541.1:c.1852G=	ENSP00000493665.1:p.Ala618=
ENST00000681521.1:c.1900G=	ENSP00000506037.1:p.Ala634=
ENST00000269197.9:c.2020G=	ENSP00000269197.4:p.Ala674=
ENST00000592288.5:c.*1144G=	ENSP00000465053.1:n.*1144G=
NM_030632.1:c.2020G=	NP_085135.1:p.Ala674=
XM_005258356.1:c.2023G=	XP_005258413.1:p.Ala675=
XM_011526205.1:c.1996G=	XP_011524507.1:p.Ala666=
XM_011526206.1:c.1942G=	XP_011524508.1:p.Ala648=
XM_011526207.1:c.1942G=	XP_011524509.1:p.Ala648=
XM_011526208.1:c.1903G=	XP_011524510.1:p.Ala635=
XM_011526209.1:c.1852G=	XP_011524511.1:p.Ala618=
XM_011526210.1:c.1852G=	XP_011524512.1:p.Ala618=
XM_011526211.1:c.1852G=	XP_011524513.1:p.Ala618=
XM_011526212.1:c.1852G=	XP_011524514.1:p.Ala618=
XM_011526213.1:c.1852G=	XP_011524515.1:p.Ala618=
XM_011526214.1:c.1852G=	XP_011524516.1:p.Ala618=
NM_030632.2:c.2020G=	NP_085135.1:p.Ala674=
XM_011526205.2:c.1996G=	XP_011524507.1:p.Ala666=
XM_011526206.2:c.1942G=	XP_011524508.1:p.Ala648=
XM_011526213.2:c.1852G=	XP_011524515.1:p.Ala618=
XM_017026012.1:c.1942G=	XP_016881501.1:p.Ala648=
XM_017026013.1:c.1852G=	XP_016881502.1:p.Ala618=
XM_017026014.2:c.1852G=	XP_016881503.1:p.Ala618=
XM_024451269.1:c.1852G=	XP_024307037.1:p.Ala618=
NM_030632.3:c.2020G= MANE Select	NP_085135.1:p.Ala674=