Canonical Allele Identifier: CA503768522

Gene: ASXL3

Linked Data

• MyVariant Identifiers: chr18:g.31319063A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33739099A>T , CM000680.2:g.33739099A>T	GRCh38
NC_000018.9:g.31319063A>T , CM000680.1:g.31319063A>T	GRCh37
NC_000018.8:g.29573061A>T	NCBI36
NG_055244.1:g.165523A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.1698A>T	ENSP00000513003.1:p.Val566=
ENST00000269197.12:c.1695A>T MANE Select	ENSP00000269197.4:p.Val565=
ENST00000592288.6:c.*819A>T	ENSP00000465053.1:n.*819A>T
ENST00000592541.6:c.*1354A>T	ENSP00000466655.2:n.*1354A>T
ENST00000593195.6:c.1907A>T	ENSP00000466073.1:n.1907A>T
ENST00000642541.1:c.1527A>T	ENSP00000493665.1:p.Val509=
ENST00000681521.1:c.1575A>T	ENSP00000506037.1:p.Val525=
ENST00000269197.9:c.1695A>T	ENSP00000269197.4:p.Val565=
ENST00000592288.5:c.*819A>T	ENSP00000465053.1:n.*819A>T
NM_030632.1:c.1695A>T	NP_085135.1:p.Val565=
XM_005258356.1:c.1698A>T	XP_005258413.1:p.Val566=
XM_011526205.1:c.1671A>T	XP_011524507.1:p.Val557=
XM_011526206.1:c.1617A>T	XP_011524508.1:p.Val539=
XM_011526207.1:c.1617A>T	XP_011524509.1:p.Val539=
XM_011526208.1:c.1578A>T	XP_011524510.1:p.Val526=
XM_011526209.1:c.1527A>T	XP_011524511.1:p.Val509=
XM_011526210.1:c.1527A>T	XP_011524512.1:p.Val509=
XM_011526211.1:c.1527A>T	XP_011524513.1:p.Val509=
XM_011526212.1:c.1527A>T	XP_011524514.1:p.Val509=
XM_011526213.1:c.1527A>T	XP_011524515.1:p.Val509=
XM_011526214.1:c.1527A>T	XP_011524516.1:p.Val509=
NM_030632.2:c.1695A>T	NP_085135.1:p.Val565=
XM_011526205.2:c.1671A>T	XP_011524507.1:p.Val557=
XM_011526206.2:c.1617A>T	XP_011524508.1:p.Val539=
XM_011526213.2:c.1527A>T	XP_011524515.1:p.Val509=
XM_017026012.1:c.1617A>T	XP_016881501.1:p.Val539=
XM_017026013.1:c.1527A>T	XP_016881502.1:p.Val509=
XM_017026014.2:c.1527A>T	XP_016881503.1:p.Val509=
XM_024451269.1:c.1527A>T	XP_024307037.1:p.Val509=
NM_030632.3:c.1695A>T MANE Select	NP_085135.1:p.Val565=