Canonical Allele Identifier: CA16044280

Gene: ASXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33739365dup , CM000680.2:g.33739365dup	GRCh38
NC_000018.9:g.31319329dup , CM000680.1:g.31319329dup	GRCh37
NC_000018.8:g.29573327dup	NCBI36
NG_055244.1:g.165789dup

Transcript Alleles

HGVS	Amino-acid Change
NM_030632.3:c.1961dup MANE Select	NP_085135.1:p.Ser655Ter
ENST00000269197.12:c.1961dup MANE Select	ENSP00000269197.4:p.Ser655Ter
NM_030632.1:c.1961dup	NP_085135.1:p.Ser655Ter
NM_030632.2:c.1961dup	NP_085135.1:p.Ser655Ter
ENST00000269197.9:c.1961dup	ENSP00000269197.4:p.Ser655Ter
ENST00000592288.5:c.*1085dup	ENSP00000465053.1:n.*1085dup
ENST00000592288.6:c.*1085dup	ENSP00000465053.1:n.*1085dup
ENST00000592541.6:c.*1620dup	ENSP00000466655.2:n.*1620dup
ENST00000593195.6:c.2173dup	ENSP00000466073.1:n.2173dup
ENST00000642541.1:c.1793dup	ENSP00000493665.1:p.Ser599Ter
ENST00000681521.1:c.1841dup	ENSP00000506037.1:p.Ser615Ter
ENST00000696964.1:c.1964dup	ENSP00000513003.1:p.Ser656Ter
XM_005258356.1:c.1964dup	XP_005258413.1:p.Ser656Ter
XM_011526205.1:c.1937dup	XP_011524507.1:p.Ser647Ter
XM_011526205.2:c.1937dup	XP_011524507.1:p.Ser647Ter
XM_011526206.1:c.1883dup	XP_011524508.1:p.Ser629Ter
XM_011526206.2:c.1883dup	XP_011524508.1:p.Ser629Ter
XM_011526207.1:c.1883dup	XP_011524509.1:p.Ser629Ter
XM_011526208.1:c.1844dup	XP_011524510.1:p.Ser616Ter
XM_011526209.1:c.1793dup	XP_011524511.1:p.Ser599Ter
XM_011526210.1:c.1793dup	XP_011524512.1:p.Ser599Ter
XM_011526211.1:c.1793dup	XP_011524513.1:p.Ser599Ter
XM_011526212.1:c.1793dup	XP_011524514.1:p.Ser599Ter
XM_011526213.1:c.1793dup	XP_011524515.1:p.Ser599Ter
XM_011526213.2:c.1793dup	XP_011524515.1:p.Ser599Ter
XM_011526214.1:c.1793dup	XP_011524516.1:p.Ser599Ter
XM_017026012.1:c.1883dup	XP_016881501.1:p.Ser629Ter
XM_017026013.1:c.1793dup	XP_016881502.1:p.Ser599Ter
XM_017026014.2:c.1793dup	XP_016881503.1:p.Ser599Ter
XM_024451269.1:c.1793dup	XP_024307037.1:p.Ser599Ter