Canonical Allele Identifier: CA503769493
Gene: ASXL3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.31322990C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.33743026C>A , CM000680.2:g.33743026C>A GRCh38
NC_000018.9:g.31322990C>A , CM000680.1:g.31322990C>A GRCh37
NC_000018.8:g.29576988C>A NCBI36
NG_055244.1:g.169450C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696964.1:c.3181C>A ENSP00000513003.1:p.Arg1061=
ENST00000269197.12:c.3178C>A MANE Select ENSP00000269197.4:p.Arg1060=
ENST00000592288.6:c.*2302C>A ENSP00000465053.1:n.*2302C>A
ENST00000592541.6:c.*2837C>A ENSP00000466655.2:n.*2837C>A
ENST00000593195.6:c.3390C>A ENSP00000466073.1:n.3390C>A
ENST00000642541.1:c.3010C>A ENSP00000493665.1:p.Arg1004=
ENST00000681521.1:c.3058C>A ENSP00000506037.1:p.Arg1020=
ENST00000269197.9:c.3178C>A ENSP00000269197.4:p.Arg1060=
ENST00000592288.5:c.*2302C>A ENSP00000465053.1:n.*2302C>A
NM_030632.1:c.3178C>A NP_085135.1:p.Arg1060=
XM_005258356.1:c.3181C>A XP_005258413.1:p.Arg1061=
XM_011526205.1:c.3154C>A XP_011524507.1:p.Arg1052=
XM_011526206.1:c.3100C>A XP_011524508.1:p.Arg1034=
XM_011526207.1:c.3100C>A XP_011524509.1:p.Arg1034=
XM_011526208.1:c.3061C>A XP_011524510.1:p.Arg1021=
XM_011526209.1:c.3010C>A XP_011524511.1:p.Arg1004=
XM_011526210.1:c.3010C>A XP_011524512.1:p.Arg1004=
XM_011526211.1:c.3010C>A XP_011524513.1:p.Arg1004=
XM_011526212.1:c.3010C>A XP_011524514.1:p.Arg1004=
XM_011526213.1:c.3010C>A XP_011524515.1:p.Arg1004=
XM_011526214.1:c.3010C>A XP_011524516.1:p.Arg1004=
XM_011526215.1:c.142C>A XP_011524517.1:p.Arg48=
NM_030632.2:c.3178C>A NP_085135.1:p.Arg1060=
XM_011526205.2:c.3154C>A XP_011524507.1:p.Arg1052=
XM_011526206.2:c.3100C>A XP_011524508.1:p.Arg1034=
XM_011526213.2:c.3010C>A XP_011524515.1:p.Arg1004=
XM_017026012.1:c.3100C>A XP_016881501.1:p.Arg1034=
XM_017026013.1:c.3010C>A XP_016881502.1:p.Arg1004=
XM_017026014.2:c.3010C>A XP_016881503.1:p.Arg1004=
XM_024451269.1:c.3010C>A XP_024307037.1:p.Arg1004=
NM_030632.3:c.3178C>A MANE Select NP_085135.1:p.Arg1060=