Canonical Allele Identifier: CA402176878

Gene: ASXL3

Linked Data

• MyVariant Identifiers: chr18:g.31319284C>A (hg19) ; chr18:g.33739320C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33739320C>A , CM000680.2:g.33739320C>A	GRCh38
NC_000018.9:g.31319284C>A , CM000680.1:g.31319284C>A	GRCh37
NC_000018.8:g.29573282C>A	NCBI36
NG_055244.1:g.165744C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.1919C>A	ENSP00000513003.1:p.Ser640Ter
ENST00000269197.12:c.1916C>A MANE Select	ENSP00000269197.4:p.Ser639Ter
ENST00000592288.6:c.*1040C>A	ENSP00000465053.1:n.*1040C>A
ENST00000592541.6:c.*1575C>A	ENSP00000466655.2:n.*1575C>A
ENST00000593195.6:c.2128C>A	ENSP00000466073.1:n.2128C>A
ENST00000642541.1:c.1748C>A	ENSP00000493665.1:p.Ser583Ter
ENST00000681521.1:c.1796C>A	ENSP00000506037.1:p.Ser599Ter
ENST00000269197.9:c.1916C>A	ENSP00000269197.4:p.Ser639Ter
ENST00000592288.5:c.*1040C>A	ENSP00000465053.1:n.*1040C>A
NM_030632.1:c.1916C>A	NP_085135.1:p.Ser639Ter
XM_005258356.1:c.1919C>A	XP_005258413.1:p.Ser640Ter
XM_011526205.1:c.1892C>A	XP_011524507.1:p.Ser631Ter
XM_011526206.1:c.1838C>A	XP_011524508.1:p.Ser613Ter
XM_011526207.1:c.1838C>A	XP_011524509.1:p.Ser613Ter
XM_011526208.1:c.1799C>A	XP_011524510.1:p.Ser600Ter
XM_011526209.1:c.1748C>A	XP_011524511.1:p.Ser583Ter
XM_011526210.1:c.1748C>A	XP_011524512.1:p.Ser583Ter
XM_011526211.1:c.1748C>A	XP_011524513.1:p.Ser583Ter
XM_011526212.1:c.1748C>A	XP_011524514.1:p.Ser583Ter
XM_011526213.1:c.1748C>A	XP_011524515.1:p.Ser583Ter
XM_011526214.1:c.1748C>A	XP_011524516.1:p.Ser583Ter
NM_030632.2:c.1916C>A	NP_085135.1:p.Ser639Ter
XM_011526205.2:c.1892C>A	XP_011524507.1:p.Ser631Ter
XM_011526206.2:c.1838C>A	XP_011524508.1:p.Ser613Ter
XM_011526213.2:c.1748C>A	XP_011524515.1:p.Ser583Ter
XM_017026012.1:c.1838C>A	XP_016881501.1:p.Ser613Ter
XM_017026013.1:c.1748C>A	XP_016881502.1:p.Ser583Ter
XM_017026014.2:c.1748C>A	XP_016881503.1:p.Ser583Ter
XM_024451269.1:c.1748C>A	XP_024307037.1:p.Ser583Ter
NM_030632.3:c.1916C>A MANE Select	NP_085135.1:p.Ser639Ter