Canonical Allele Identifier: CA402176490
Gene: ASXL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.33739239C>T , CM000680.2:g.33739239C>T GRCh38
NC_000018.9:g.31319203C>T , CM000680.1:g.31319203C>T GRCh37
NC_000018.8:g.29573201C>T NCBI36
NG_055244.1:g.165663C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696964.1:c.1838C>T ENSP00000513003.1:p.Ser613Phe
ENST00000269197.12:c.1835C>T MANE Select ENSP00000269197.4:p.Ser612Phe
ENST00000592288.6:c.*959C>T ENSP00000465053.1:n.*959C>T
ENST00000592541.6:c.*1494C>T ENSP00000466655.2:n.*1494C>T
ENST00000593195.6:c.2047C>T ENSP00000466073.1:n.2047C>T
ENST00000642541.1:c.1667C>T ENSP00000493665.1:p.Ser556Phe
ENST00000681521.1:c.1715C>T ENSP00000506037.1:p.Ser572Phe
ENST00000269197.9:c.1835C>T ENSP00000269197.4:p.Ser612Phe
ENST00000592288.5:c.*959C>T ENSP00000465053.1:n.*959C>T
NM_030632.1:c.1835C>T NP_085135.1:p.Ser612Phe
XM_005258356.1:c.1838C>T XP_005258413.1:p.Ser613Phe
XM_011526205.1:c.1811C>T XP_011524507.1:p.Ser604Phe
XM_011526206.1:c.1757C>T XP_011524508.1:p.Ser586Phe
XM_011526207.1:c.1757C>T XP_011524509.1:p.Ser586Phe
XM_011526208.1:c.1718C>T XP_011524510.1:p.Ser573Phe
XM_011526209.1:c.1667C>T XP_011524511.1:p.Ser556Phe
XM_011526210.1:c.1667C>T XP_011524512.1:p.Ser556Phe
XM_011526211.1:c.1667C>T XP_011524513.1:p.Ser556Phe
XM_011526212.1:c.1667C>T XP_011524514.1:p.Ser556Phe
XM_011526213.1:c.1667C>T XP_011524515.1:p.Ser556Phe
XM_011526214.1:c.1667C>T XP_011524516.1:p.Ser556Phe
NM_030632.2:c.1835C>T NP_085135.1:p.Ser612Phe
XM_011526205.2:c.1811C>T XP_011524507.1:p.Ser604Phe
XM_011526206.2:c.1757C>T XP_011524508.1:p.Ser586Phe
XM_011526213.2:c.1667C>T XP_011524515.1:p.Ser556Phe
XM_017026012.1:c.1757C>T XP_016881501.1:p.Ser586Phe
XM_017026013.1:c.1667C>T XP_016881502.1:p.Ser556Phe
XM_017026014.2:c.1667C>T XP_016881503.1:p.Ser556Phe
XM_024451269.1:c.1667C>T XP_024307037.1:p.Ser556Phe
NM_030632.3:c.1835C>T MANE Select NP_085135.1:p.Ser612Phe