Canonical Allele Identifier: CA353436
Gene: ASXL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 224134
ClinVar RCV Id: RCV000209910
dbSNP Id: rs869312696

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.33739086C>A , CM000680.2:g.33739086C>A GRCh38
NC_000018.9:g.31319050C>A , CM000680.1:g.31319050C>A GRCh37
NC_000018.8:g.29573048C>A NCBI36
NG_055244.1:g.165510C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696964.1:c.1685C>A ENSP00000513003.1:p.Ser562Ter
ENST00000269197.12:c.1682C>A MANE Select ENSP00000269197.4:p.Ser561Ter
ENST00000592288.6:c.*806C>A ENSP00000465053.1:n.*806C>A
ENST00000592541.6:c.*1341C>A ENSP00000466655.2:n.*1341C>A
ENST00000593195.6:c.1894C>A ENSP00000466073.1:n.1894C>A
ENST00000642541.1:c.1514C>A ENSP00000493665.1:p.Ser505Ter
ENST00000681521.1:c.1562C>A ENSP00000506037.1:p.Ser521Ter
ENST00000269197.9:c.1682C>A ENSP00000269197.4:p.Ser561Ter
ENST00000592288.5:c.*806C>A ENSP00000465053.1:n.*806C>A
NM_030632.1:c.1682C>A NP_085135.1:p.Ser561Ter
XM_005258356.1:c.1685C>A XP_005258413.1:p.Ser562Ter
XM_011526205.1:c.1658C>A XP_011524507.1:p.Ser553Ter
XM_011526206.1:c.1604C>A XP_011524508.1:p.Ser535Ter
XM_011526207.1:c.1604C>A XP_011524509.1:p.Ser535Ter
XM_011526208.1:c.1565C>A XP_011524510.1:p.Ser522Ter
XM_011526209.1:c.1514C>A XP_011524511.1:p.Ser505Ter
XM_011526210.1:c.1514C>A XP_011524512.1:p.Ser505Ter
XM_011526211.1:c.1514C>A XP_011524513.1:p.Ser505Ter
XM_011526212.1:c.1514C>A XP_011524514.1:p.Ser505Ter
XM_011526213.1:c.1514C>A XP_011524515.1:p.Ser505Ter
XM_011526214.1:c.1514C>A XP_011524516.1:p.Ser505Ter
NM_030632.2:c.1682C>A NP_085135.1:p.Ser561Ter
XM_011526205.2:c.1658C>A XP_011524507.1:p.Ser553Ter
XM_011526206.2:c.1604C>A XP_011524508.1:p.Ser535Ter
XM_011526213.2:c.1514C>A XP_011524515.1:p.Ser505Ter
XM_017026012.1:c.1604C>A XP_016881501.1:p.Ser535Ter
XM_017026013.1:c.1514C>A XP_016881502.1:p.Ser505Ter
XM_017026014.2:c.1514C>A XP_016881503.1:p.Ser505Ter
XM_024451269.1:c.1514C>A XP_024307037.1:p.Ser505Ter
NM_030632.3:c.1682C>A MANE Select NP_085135.1:p.Ser561Ter