Canonical Allele Identifier: CA2294857913

Gene: ASXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33743941A= , CM000680.2:g.33743941A=	GRCh38
NC_000018.9:g.31323905A= , CM000680.1:g.31323905A=	GRCh37
NC_000018.8:g.29577903A=	NCBI36
NG_055244.1:g.170365A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.4096A=	ENSP00000513003.1:p.Ile1366=
ENST00000269197.12:c.4093A= MANE Select	ENSP00000269197.4:p.Ile1365=
ENST00000681521.1:c.3973A=	ENSP00000506037.1:p.Ile1325=
ENST00000269197.9:c.4093A=	ENSP00000269197.4:p.Ile1365=
NM_030632.1:c.4093A=	NP_085135.1:p.Ile1365=
XM_005258356.1:c.4096A=	XP_005258413.1:p.Ile1366=
XM_011526205.1:c.4069A=	XP_011524507.1:p.Ile1357=
XM_011526206.1:c.4015A=	XP_011524508.1:p.Ile1339=
XM_011526207.1:c.4015A=	XP_011524509.1:p.Ile1339=
XM_011526208.1:c.3976A=	XP_011524510.1:p.Ile1326=
XM_011526209.1:c.3925A=	XP_011524511.1:p.Ile1309=
XM_011526210.1:c.3925A=	XP_011524512.1:p.Ile1309=
XM_011526211.1:c.3925A=	XP_011524513.1:p.Ile1309=
XM_011526212.1:c.3925A=	XP_011524514.1:p.Ile1309=
XM_011526213.1:c.3925A=	XP_011524515.1:p.Ile1309=
XM_011526214.1:c.3925A=	XP_011524516.1:p.Ile1309=
XM_011526215.1:c.1057A=	XP_011524517.1:p.Ile353=
NM_030632.2:c.4093A=	NP_085135.1:p.Ile1365=
XM_011526205.2:c.4069A=	XP_011524507.1:p.Ile1357=
XM_011526206.2:c.4015A=	XP_011524508.1:p.Ile1339=
XM_011526213.2:c.3925A=	XP_011524515.1:p.Ile1309=
XM_017026012.1:c.4015A=	XP_016881501.1:p.Ile1339=
XM_017026013.1:c.3925A=	XP_016881502.1:p.Ile1309=
XM_017026014.2:c.3925A=	XP_016881503.1:p.Ile1309=
XM_024451269.1:c.3925A=	XP_024307037.1:p.Ile1309=
NM_030632.3:c.4093A= MANE Select	NP_085135.1:p.Ile1365=