Canonical Allele Identifier: CA402176751
Gene: ASXL3 HGNC NCBI

Linked Data

dbSNP Id: rs1398912287

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.33739289G>A , CM000680.2:g.33739289G>A GRCh38
NC_000018.9:g.31319253G>A , CM000680.1:g.31319253G>A GRCh37
NC_000018.8:g.29573251G>A NCBI36
NG_055244.1:g.165713G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696964.1:c.1888G>A ENSP00000513003.1:p.Gly630Arg
ENST00000269197.12:c.1885G>A MANE Select ENSP00000269197.4:p.Gly629Arg
ENST00000592288.6:c.*1009G>A ENSP00000465053.1:n.*1009G>A
ENST00000592541.6:c.*1544G>A ENSP00000466655.2:n.*1544G>A
ENST00000593195.6:c.2097G>A ENSP00000466073.1:n.2097G>A
ENST00000642541.1:c.1717G>A ENSP00000493665.1:p.Gly573Arg
ENST00000681521.1:c.1765G>A ENSP00000506037.1:p.Gly589Arg
ENST00000269197.9:c.1885G>A ENSP00000269197.4:p.Gly629Arg
ENST00000592288.5:c.*1009G>A ENSP00000465053.1:n.*1009G>A
NM_030632.1:c.1885G>A NP_085135.1:p.Gly629Arg
XM_005258356.1:c.1888G>A XP_005258413.1:p.Gly630Arg
XM_011526205.1:c.1861G>A XP_011524507.1:p.Gly621Arg
XM_011526206.1:c.1807G>A XP_011524508.1:p.Gly603Arg
XM_011526207.1:c.1807G>A XP_011524509.1:p.Gly603Arg
XM_011526208.1:c.1768G>A XP_011524510.1:p.Gly590Arg
XM_011526209.1:c.1717G>A XP_011524511.1:p.Gly573Arg
XM_011526210.1:c.1717G>A XP_011524512.1:p.Gly573Arg
XM_011526211.1:c.1717G>A XP_011524513.1:p.Gly573Arg
XM_011526212.1:c.1717G>A XP_011524514.1:p.Gly573Arg
XM_011526213.1:c.1717G>A XP_011524515.1:p.Gly573Arg
XM_011526214.1:c.1717G>A XP_011524516.1:p.Gly573Arg
NM_030632.2:c.1885G>A NP_085135.1:p.Gly629Arg
XM_011526205.2:c.1861G>A XP_011524507.1:p.Gly621Arg
XM_011526206.2:c.1807G>A XP_011524508.1:p.Gly603Arg
XM_011526213.2:c.1717G>A XP_011524515.1:p.Gly573Arg
XM_017026012.1:c.1807G>A XP_016881501.1:p.Gly603Arg
XM_017026013.1:c.1717G>A XP_016881502.1:p.Gly573Arg
XM_017026014.2:c.1717G>A XP_016881503.1:p.Gly573Arg
XM_024451269.1:c.1717G>A XP_024307037.1:p.Gly573Arg
NM_030632.3:c.1885G>A MANE Select NP_085135.1:p.Gly629Arg