Canonical Allele Identifier: CA402175568
Gene: ASXL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.33738890G>A , CM000680.2:g.33738890G>A GRCh38
NC_000018.9:g.31318854G>A , CM000680.1:g.31318854G>A GRCh37
NC_000018.8:g.29572852G>A NCBI36
NG_055244.1:g.165314G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696964.1:c.1489G>A ENSP00000513003.1:p.Glu497Lys
ENST00000269197.12:c.1486G>A MANE Select ENSP00000269197.4:p.Glu496Lys
ENST00000592288.6:c.*610G>A ENSP00000465053.1:n.*610G>A
ENST00000592541.6:c.*1145G>A ENSP00000466655.2:n.*1145G>A
ENST00000593195.6:c.1698G>A ENSP00000466073.1:n.1698G>A
ENST00000642541.1:c.1318G>A ENSP00000493665.1:p.Glu440Lys
ENST00000681521.1:c.1366G>A ENSP00000506037.1:p.Glu456Lys
ENST00000269197.9:c.1486G>A ENSP00000269197.4:p.Glu496Lys
ENST00000592288.5:c.*610G>A ENSP00000465053.1:n.*610G>A
NM_030632.1:c.1486G>A NP_085135.1:p.Glu496Lys
XM_005258356.1:c.1489G>A XP_005258413.1:p.Glu497Lys
XM_011526205.1:c.1462G>A XP_011524507.1:p.Glu488Lys
XM_011526206.1:c.1408G>A XP_011524508.1:p.Glu470Lys
XM_011526207.1:c.1408G>A XP_011524509.1:p.Glu470Lys
XM_011526208.1:c.1369G>A XP_011524510.1:p.Glu457Lys
XM_011526209.1:c.1318G>A XP_011524511.1:p.Glu440Lys
XM_011526210.1:c.1318G>A XP_011524512.1:p.Glu440Lys
XM_011526211.1:c.1318G>A XP_011524513.1:p.Glu440Lys
XM_011526212.1:c.1318G>A XP_011524514.1:p.Glu440Lys
XM_011526213.1:c.1318G>A XP_011524515.1:p.Glu440Lys
XM_011526214.1:c.1318G>A XP_011524516.1:p.Glu440Lys
NM_030632.2:c.1486G>A NP_085135.1:p.Glu496Lys
XM_011526205.2:c.1462G>A XP_011524507.1:p.Glu488Lys
XM_011526206.2:c.1408G>A XP_011524508.1:p.Glu470Lys
XM_011526213.2:c.1318G>A XP_011524515.1:p.Glu440Lys
XM_017026012.1:c.1408G>A XP_016881501.1:p.Glu470Lys
XM_017026013.1:c.1318G>A XP_016881502.1:p.Glu440Lys
XM_017026014.2:c.1318G>A XP_016881503.1:p.Glu440Lys
XM_024451269.1:c.1318G>A XP_024307037.1:p.Glu440Lys
NM_030632.3:c.1486G>A MANE Select NP_085135.1:p.Glu496Lys