Canonical Allele Identifier: CA2294857559
Gene: ASXL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.33743116C= , CM000680.2:g.33743116C= GRCh38
NC_000018.9:g.31323080C= , CM000680.1:g.31323080C= GRCh37
NC_000018.8:g.29577078C= NCBI36
NG_055244.1:g.169540C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696964.1:c.3271C= ENSP00000513003.1:p.Pro1091=
ENST00000269197.12:c.3268C= MANE Select ENSP00000269197.4:p.Pro1090=
ENST00000592288.6:c.*2392C= ENSP00000465053.1:n.*2392C=
ENST00000592541.6:c.*2927C= ENSP00000466655.2:n.*2927C=
ENST00000593195.6:c.3480C= ENSP00000466073.1:n.3480C=
ENST00000642541.1:c.3100C= ENSP00000493665.1:p.Pro1034=
ENST00000681521.1:c.3148C= ENSP00000506037.1:p.Pro1050=
ENST00000269197.9:c.3268C= ENSP00000269197.4:p.Pro1090=
ENST00000592288.5:c.*2392C= ENSP00000465053.1:n.*2392C=
NM_030632.1:c.3268C= NP_085135.1:p.Pro1090=
XM_005258356.1:c.3271C= XP_005258413.1:p.Pro1091=
XM_011526205.1:c.3244C= XP_011524507.1:p.Pro1082=
XM_011526206.1:c.3190C= XP_011524508.1:p.Pro1064=
XM_011526207.1:c.3190C= XP_011524509.1:p.Pro1064=
XM_011526208.1:c.3151C= XP_011524510.1:p.Pro1051=
XM_011526209.1:c.3100C= XP_011524511.1:p.Pro1034=
XM_011526210.1:c.3100C= XP_011524512.1:p.Pro1034=
XM_011526211.1:c.3100C= XP_011524513.1:p.Pro1034=
XM_011526212.1:c.3100C= XP_011524514.1:p.Pro1034=
XM_011526213.1:c.3100C= XP_011524515.1:p.Pro1034=
XM_011526214.1:c.3100C= XP_011524516.1:p.Pro1034=
XM_011526215.1:c.232C= XP_011524517.1:p.Pro78=
NM_030632.2:c.3268C= NP_085135.1:p.Pro1090=
XM_011526205.2:c.3244C= XP_011524507.1:p.Pro1082=
XM_011526206.2:c.3190C= XP_011524508.1:p.Pro1064=
XM_011526213.2:c.3100C= XP_011524515.1:p.Pro1034=
XM_017026012.1:c.3190C= XP_016881501.1:p.Pro1064=
XM_017026013.1:c.3100C= XP_016881502.1:p.Pro1034=
XM_017026014.2:c.3100C= XP_016881503.1:p.Pro1034=
XM_024451269.1:c.3100C= XP_024307037.1:p.Pro1034=
NM_030632.3:c.3268C= MANE Select NP_085135.1:p.Pro1090=