Canonical Allele Identifier: CA2294855978

Gene: ASXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33739440_33739449delinsAAATATCTCC , CM000680.2:g.33739440_33739449delinsAAATATCTCC	GRCh38
NC_000018.9:g.31319404_31319413delinsAAATATCTCC , CM000680.1:g.31319404_31319413delinsAAATATCTCC	GRCh37
NC_000018.8:g.29573402_29573411delinsAAATATCTCC	NCBI36
NG_055244.1:g.165864_165873delinsAAATATCTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.2039_2048delinsAAATATCTCC	ENSP00000513003.1:p.Glu680=
ENST00000269197.12:c.2036_2045delinsAAATATCTCC MANE Select	ENSP00000269197.4:p.Glu679=
ENST00000592288.6:c.*1160_*1169delinsAAATATCTCC	ENSP00000465053.1:n.*1160_*1169delinsAAATATCTCC
ENST00000592541.6:c.*1695_*1704delinsAAATATCTCC	ENSP00000466655.2:n.*1695_*1704delinsAAATATCTCC
ENST00000593195.6:c.2248_2257delinsAAATATCTCC	ENSP00000466073.1:n.2248_2257delinsAAATATCTCC
ENST00000642541.1:c.1868_1877delinsAAATATCTCC	ENSP00000493665.1:p.Glu623=
ENST00000681521.1:c.1916_1925delinsAAATATCTCC	ENSP00000506037.1:p.Glu639=
ENST00000269197.9:c.2036_2045delinsAAATATCTCC	ENSP00000269197.4:p.Glu679=
ENST00000592288.5:c.*1160_*1169delinsAAATATCTCC	ENSP00000465053.1:n.*1160_*1169delinsAAATATCTCC
NM_030632.1:c.2036_2045delinsAAATATCTCC	NP_085135.1:p.Glu679=
XM_005258356.1:c.2039_2048delinsAAATATCTCC	XP_005258413.1:p.Glu680=
XM_011526205.1:c.2012_2021delinsAAATATCTCC	XP_011524507.1:p.Glu671=
XM_011526206.1:c.1958_1967delinsAAATATCTCC	XP_011524508.1:p.Glu653=
XM_011526207.1:c.1958_1967delinsAAATATCTCC	XP_011524509.1:p.Glu653=
XM_011526208.1:c.1919_1928delinsAAATATCTCC	XP_011524510.1:p.Glu640=
XM_011526209.1:c.1868_1877delinsAAATATCTCC	XP_011524511.1:p.Glu623=
XM_011526210.1:c.1868_1877delinsAAATATCTCC	XP_011524512.1:p.Glu623=
XM_011526211.1:c.1868_1877delinsAAATATCTCC	XP_011524513.1:p.Glu623=
XM_011526212.1:c.1868_1877delinsAAATATCTCC	XP_011524514.1:p.Glu623=
XM_011526213.1:c.1868_1877delinsAAATATCTCC	XP_011524515.1:p.Glu623=
XM_011526214.1:c.1868_1877delinsAAATATCTCC	XP_011524516.1:p.Glu623=
NM_030632.2:c.2036_2045delinsAAATATCTCC	NP_085135.1:p.Glu679=
XM_011526205.2:c.2012_2021delinsAAATATCTCC	XP_011524507.1:p.Glu671=
XM_011526206.2:c.1958_1967delinsAAATATCTCC	XP_011524508.1:p.Glu653=
XM_011526213.2:c.1868_1877delinsAAATATCTCC	XP_011524515.1:p.Glu623=
XM_017026012.1:c.1958_1967delinsAAATATCTCC	XP_016881501.1:p.Glu653=
XM_017026013.1:c.1868_1877delinsAAATATCTCC	XP_016881502.1:p.Glu623=
XM_017026014.2:c.1868_1877delinsAAATATCTCC	XP_016881503.1:p.Glu623=
XM_024451269.1:c.1868_1877delinsAAATATCTCC	XP_024307037.1:p.Glu623=
NM_030632.3:c.2036_2045delinsAAATATCTCC MANE Select	NP_085135.1:p.Glu679=