Canonical Allele Identifier: CA2294855900

Gene: ASXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33739280C= , CM000680.2:g.33739280C=	GRCh38
NC_000018.9:g.31319244C= , CM000680.1:g.31319244C=	GRCh37
NC_000018.8:g.29573242C=	NCBI36
NG_055244.1:g.165704C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.1879C=	ENSP00000513003.1:p.Pro627=
ENST00000269197.12:c.1876C= MANE Select	ENSP00000269197.4:p.Pro626=
ENST00000592288.6:c.*1000C=	ENSP00000465053.1:n.*1000C=
ENST00000592541.6:c.*1535C=	ENSP00000466655.2:n.*1535C=
ENST00000593195.6:c.2088C=	ENSP00000466073.1:n.2088C=
ENST00000642541.1:c.1708C=	ENSP00000493665.1:p.Pro570=
ENST00000681521.1:c.1756C=	ENSP00000506037.1:p.Pro586=
ENST00000269197.9:c.1876C=	ENSP00000269197.4:p.Pro626=
ENST00000592288.5:c.*1000C=	ENSP00000465053.1:n.*1000C=
NM_030632.1:c.1876C=	NP_085135.1:p.Pro626=
XM_005258356.1:c.1879C=	XP_005258413.1:p.Pro627=
XM_011526205.1:c.1852C=	XP_011524507.1:p.Pro618=
XM_011526206.1:c.1798C=	XP_011524508.1:p.Pro600=
XM_011526207.1:c.1798C=	XP_011524509.1:p.Pro600=
XM_011526208.1:c.1759C=	XP_011524510.1:p.Pro587=
XM_011526209.1:c.1708C=	XP_011524511.1:p.Pro570=
XM_011526210.1:c.1708C=	XP_011524512.1:p.Pro570=
XM_011526211.1:c.1708C=	XP_011524513.1:p.Pro570=
XM_011526212.1:c.1708C=	XP_011524514.1:p.Pro570=
XM_011526213.1:c.1708C=	XP_011524515.1:p.Pro570=
XM_011526214.1:c.1708C=	XP_011524516.1:p.Pro570=
NM_030632.2:c.1876C=	NP_085135.1:p.Pro626=
XM_011526205.2:c.1852C=	XP_011524507.1:p.Pro618=
XM_011526206.2:c.1798C=	XP_011524508.1:p.Pro600=
XM_011526213.2:c.1708C=	XP_011524515.1:p.Pro570=
XM_017026012.1:c.1798C=	XP_016881501.1:p.Pro600=
XM_017026013.1:c.1708C=	XP_016881502.1:p.Pro570=
XM_017026014.2:c.1708C=	XP_016881503.1:p.Pro570=
XM_024451269.1:c.1708C=	XP_024307037.1:p.Pro570=
NM_030632.3:c.1876C= MANE Select	NP_085135.1:p.Pro626=