Canonical Allele Identifier: CA2294855948

Gene: ASXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33739369C= , CM000680.2:g.33739369C=	GRCh38
NC_000018.9:g.31319333C= , CM000680.1:g.31319333C=	GRCh37
NC_000018.8:g.29573331C=	NCBI36
NG_055244.1:g.165793C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.1968C=	ENSP00000513003.1:p.Ser656=
ENST00000269197.12:c.1965C= MANE Select	ENSP00000269197.4:p.Ser655=
ENST00000592288.6:c.*1089C=	ENSP00000465053.1:n.*1089C=
ENST00000592541.6:c.*1624C=	ENSP00000466655.2:n.*1624C=
ENST00000593195.6:c.2177C=	ENSP00000466073.1:n.2177C=
ENST00000642541.1:c.1797C=	ENSP00000493665.1:p.Ser599=
ENST00000681521.1:c.1845C=	ENSP00000506037.1:p.Ser615=
ENST00000269197.9:c.1965C=	ENSP00000269197.4:p.Ser655=
ENST00000592288.5:c.*1089C=	ENSP00000465053.1:n.*1089C=
NM_030632.1:c.1965C=	NP_085135.1:p.Ser655=
XM_005258356.1:c.1968C=	XP_005258413.1:p.Ser656=
XM_011526205.1:c.1941C=	XP_011524507.1:p.Ser647=
XM_011526206.1:c.1887C=	XP_011524508.1:p.Ser629=
XM_011526207.1:c.1887C=	XP_011524509.1:p.Ser629=
XM_011526208.1:c.1848C=	XP_011524510.1:p.Ser616=
XM_011526209.1:c.1797C=	XP_011524511.1:p.Ser599=
XM_011526210.1:c.1797C=	XP_011524512.1:p.Ser599=
XM_011526211.1:c.1797C=	XP_011524513.1:p.Ser599=
XM_011526212.1:c.1797C=	XP_011524514.1:p.Ser599=
XM_011526213.1:c.1797C=	XP_011524515.1:p.Ser599=
XM_011526214.1:c.1797C=	XP_011524516.1:p.Ser599=
NM_030632.2:c.1965C=	NP_085135.1:p.Ser655=
XM_011526205.2:c.1941C=	XP_011524507.1:p.Ser647=
XM_011526206.2:c.1887C=	XP_011524508.1:p.Ser629=
XM_011526213.2:c.1797C=	XP_011524515.1:p.Ser599=
XM_017026012.1:c.1887C=	XP_016881501.1:p.Ser629=
XM_017026013.1:c.1797C=	XP_016881502.1:p.Ser599=
XM_017026014.2:c.1797C=	XP_016881503.1:p.Ser599=
XM_024451269.1:c.1797C=	XP_024307037.1:p.Ser599=
NM_030632.3:c.1965C= MANE Select	NP_085135.1:p.Ser655=