Canonical Allele Identifier: CA503768600

Gene: ASXL3

Linked Data

• MyVariant Identifiers: chr18:g.31319103C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33739139C>T , CM000680.2:g.33739139C>T	GRCh38
NC_000018.9:g.31319103C>T , CM000680.1:g.31319103C>T	GRCh37
NC_000018.8:g.29573101C>T	NCBI36
NG_055244.1:g.165563C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.1738C>T	ENSP00000513003.1:p.Leu580=
ENST00000269197.12:c.1735C>T MANE Select	ENSP00000269197.4:p.Leu579=
ENST00000592288.6:c.*859C>T	ENSP00000465053.1:n.*859C>T
ENST00000592541.6:c.*1394C>T	ENSP00000466655.2:n.*1394C>T
ENST00000593195.6:c.1947C>T	ENSP00000466073.1:n.1947C>T
ENST00000642541.1:c.1567C>T	ENSP00000493665.1:p.Leu523=
ENST00000681521.1:c.1615C>T	ENSP00000506037.1:p.Leu539=
ENST00000269197.9:c.1735C>T	ENSP00000269197.4:p.Leu579=
ENST00000592288.5:c.*859C>T	ENSP00000465053.1:n.*859C>T
NM_030632.1:c.1735C>T	NP_085135.1:p.Leu579=
XM_005258356.1:c.1738C>T	XP_005258413.1:p.Leu580=
XM_011526205.1:c.1711C>T	XP_011524507.1:p.Leu571=
XM_011526206.1:c.1657C>T	XP_011524508.1:p.Leu553=
XM_011526207.1:c.1657C>T	XP_011524509.1:p.Leu553=
XM_011526208.1:c.1618C>T	XP_011524510.1:p.Leu540=
XM_011526209.1:c.1567C>T	XP_011524511.1:p.Leu523=
XM_011526210.1:c.1567C>T	XP_011524512.1:p.Leu523=
XM_011526211.1:c.1567C>T	XP_011524513.1:p.Leu523=
XM_011526212.1:c.1567C>T	XP_011524514.1:p.Leu523=
XM_011526213.1:c.1567C>T	XP_011524515.1:p.Leu523=
XM_011526214.1:c.1567C>T	XP_011524516.1:p.Leu523=
NM_030632.2:c.1735C>T	NP_085135.1:p.Leu579=
XM_011526205.2:c.1711C>T	XP_011524507.1:p.Leu571=
XM_011526206.2:c.1657C>T	XP_011524508.1:p.Leu553=
XM_011526213.2:c.1567C>T	XP_011524515.1:p.Leu523=
XM_017026012.1:c.1657C>T	XP_016881501.1:p.Leu553=
XM_017026013.1:c.1567C>T	XP_016881502.1:p.Leu523=
XM_017026014.2:c.1567C>T	XP_016881503.1:p.Leu523=
XM_024451269.1:c.1567C>T	XP_024307037.1:p.Leu523=
NM_030632.3:c.1735C>T MANE Select	NP_085135.1:p.Leu579=