Canonical Allele Identifier: CA645603028
Gene: ASXL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.33743784del , CM000680.2:g.33743784del GRCh38
NC_000018.9:g.31323748del , CM000680.1:g.31323748del GRCh37
NC_000018.8:g.29577746del NCBI36
NG_055244.1:g.170208del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696964.1:c.3939del ENSP00000513003.1:p.Ser1314AlafsTer12
ENST00000269197.12:c.3936del MANE Select ENSP00000269197.4:p.Ser1313AlafsTer12
ENST00000681521.1:c.3816del ENSP00000506037.1:p.Ser1273AlafsTer12
ENST00000269197.9:c.3936del ENSP00000269197.4:p.Ser1313AlafsTer12
NM_030632.1:c.3936del NP_085135.1:p.Ser1313AlafsTer12
XM_005258356.1:c.3939del XP_005258413.1:p.Ser1314AlafsTer12
XM_011526205.1:c.3912del XP_011524507.1:p.Ser1305AlafsTer12
XM_011526206.1:c.3858del XP_011524508.1:p.Ser1287AlafsTer12
XM_011526207.1:c.3858del XP_011524509.1:p.Ser1287AlafsTer12
XM_011526208.1:c.3819del XP_011524510.1:p.Ser1274AlafsTer12
XM_011526209.1:c.3768del XP_011524511.1:p.Ser1257AlafsTer12
XM_011526210.1:c.3768del XP_011524512.1:p.Ser1257AlafsTer12
XM_011526211.1:c.3768del XP_011524513.1:p.Ser1257AlafsTer12
XM_011526212.1:c.3768del XP_011524514.1:p.Ser1257AlafsTer12
XM_011526213.1:c.3768del XP_011524515.1:p.Ser1257AlafsTer12
XM_011526214.1:c.3768del XP_011524516.1:p.Ser1257AlafsTer12
XM_011526215.1:c.900del XP_011524517.1:p.Ser301AlafsTer12
NM_030632.2:c.3936del NP_085135.1:p.Ser1313AlafsTer12
XM_011526205.2:c.3912del XP_011524507.1:p.Ser1305AlafsTer12
XM_011526206.2:c.3858del XP_011524508.1:p.Ser1287AlafsTer12
XM_011526213.2:c.3768del XP_011524515.1:p.Ser1257AlafsTer12
XM_017026012.1:c.3858del XP_016881501.1:p.Ser1287AlafsTer12
XM_017026013.1:c.3768del XP_016881502.1:p.Ser1257AlafsTer12
XM_017026014.2:c.3768del XP_016881503.1:p.Ser1257AlafsTer12
XM_024451269.1:c.3768del XP_024307037.1:p.Ser1257AlafsTer12
NM_030632.3:c.3936del MANE Select NP_085135.1:p.Ser1313AlafsTer12