Canonical Allele Identifier: CA2294855698

Gene: ASXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33738826T= , CM000680.2:g.33738826T=	GRCh38
NC_000018.9:g.31318790T= , CM000680.1:g.31318790T=	GRCh37
NC_000018.8:g.29572788T=	NCBI36
NG_055244.1:g.165250T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.1425T=	ENSP00000513003.1:p.Pro475=
ENST00000269197.12:c.1422T= MANE Select	ENSP00000269197.4:p.Pro474=
ENST00000592288.6:c.*546T=	ENSP00000465053.1:n.*546T=
ENST00000592541.6:c.*1081T=	ENSP00000466655.2:n.*1081T=
ENST00000593195.6:c.1634T=	ENSP00000466073.1:n.1634T=
ENST00000642541.1:c.1254T=	ENSP00000493665.1:p.Pro418=
ENST00000681521.1:c.1302T=	ENSP00000506037.1:p.Pro434=
ENST00000269197.9:c.1422T=	ENSP00000269197.4:p.Pro474=
ENST00000592288.5:c.*546T=	ENSP00000465053.1:n.*546T=
NM_030632.1:c.1422T=	NP_085135.1:p.Pro474=
XM_005258356.1:c.1425T=	XP_005258413.1:p.Pro475=
XM_011526205.1:c.1398T=	XP_011524507.1:p.Pro466=
XM_011526206.1:c.1344T=	XP_011524508.1:p.Pro448=
XM_011526207.1:c.1344T=	XP_011524509.1:p.Pro448=
XM_011526208.1:c.1305T=	XP_011524510.1:p.Pro435=
XM_011526209.1:c.1254T=	XP_011524511.1:p.Pro418=
XM_011526210.1:c.1254T=	XP_011524512.1:p.Pro418=
XM_011526211.1:c.1254T=	XP_011524513.1:p.Pro418=
XM_011526212.1:c.1254T=	XP_011524514.1:p.Pro418=
XM_011526213.1:c.1254T=	XP_011524515.1:p.Pro418=
XM_011526214.1:c.1254T=	XP_011524516.1:p.Pro418=
NM_030632.2:c.1422T=	NP_085135.1:p.Pro474=
XM_011526205.2:c.1398T=	XP_011524507.1:p.Pro466=
XM_011526206.2:c.1344T=	XP_011524508.1:p.Pro448=
XM_011526213.2:c.1254T=	XP_011524515.1:p.Pro418=
XM_017026012.1:c.1344T=	XP_016881501.1:p.Pro448=
XM_017026013.1:c.1254T=	XP_016881502.1:p.Pro418=
XM_017026014.2:c.1254T=	XP_016881503.1:p.Pro418=
XM_024451269.1:c.1254T=	XP_024307037.1:p.Pro418=
NM_030632.3:c.1422T= MANE Select	NP_085135.1:p.Pro474=