Canonical Allele Identifier: CA2294858200
Gene: ASXL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.33744578A= , CM000680.2:g.33744578A= GRCh38
NC_000018.9:g.31324542A= , CM000680.1:g.31324542A= GRCh37
NC_000018.8:g.29578540A= NCBI36
NG_055244.1:g.171002A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696964.1:c.4733A= ENSP00000513003.1:p.His1578=
ENST00000269197.12:c.4730A= MANE Select ENSP00000269197.4:p.His1577=
ENST00000681521.1:c.4610A= ENSP00000506037.1:p.His1537=
ENST00000269197.9:c.4730A= ENSP00000269197.4:p.His1577=
NM_030632.1:c.4730A= NP_085135.1:p.His1577=
XM_005258356.1:c.4733A= XP_005258413.1:p.His1578=
XM_011526205.1:c.4706A= XP_011524507.1:p.His1569=
XM_011526206.1:c.4652A= XP_011524508.1:p.His1551=
XM_011526207.1:c.4652A= XP_011524509.1:p.His1551=
XM_011526208.1:c.4613A= XP_011524510.1:p.His1538=
XM_011526209.1:c.4562A= XP_011524511.1:p.His1521=
XM_011526210.1:c.4562A= XP_011524512.1:p.His1521=
XM_011526211.1:c.4562A= XP_011524513.1:p.His1521=
XM_011526212.1:c.4562A= XP_011524514.1:p.His1521=
XM_011526213.1:c.4562A= XP_011524515.1:p.His1521=
XM_011526214.1:c.4562A= XP_011524516.1:p.His1521=
XM_011526215.1:c.1694A= XP_011524517.1:p.His565=
NM_030632.2:c.4730A= NP_085135.1:p.His1577=
XM_011526205.2:c.4706A= XP_011524507.1:p.His1569=
XM_011526206.2:c.4652A= XP_011524508.1:p.His1551=
XM_011526213.2:c.4562A= XP_011524515.1:p.His1521=
XM_017026012.1:c.4652A= XP_016881501.1:p.His1551=
XM_017026013.1:c.4562A= XP_016881502.1:p.His1521=
XM_017026014.2:c.4562A= XP_016881503.1:p.His1521=
XM_024451269.1:c.4562A= XP_024307037.1:p.His1521=
NM_030632.3:c.4730A= MANE Select NP_085135.1:p.His1577=