Canonical Allele Identifier: CA658791347

Gene: ASXL3

Linked Data

• PubMed: PMID:28135719

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33738889_33738892dup , CM000680.2:g.33738889_33738892dup	GRCh38
NC_000018.9:g.31318853_31318856dup , CM000680.1:g.31318853_31318856dup	GRCh37
NC_000018.8:g.29572851_29572854dup	NCBI36
NG_055244.1:g.165313_165316dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.1488_1491dup	ENSP00000513003.1:p.Asp498Ter
ENST00000269197.12:c.1485_1488dup MANE Select	ENSP00000269197.4:p.Asp497Ter
ENST00000592288.6:c.*609_*612dup	ENSP00000465053.1:n.*609_*612dup
ENST00000592541.6:c.*1144_*1147dup	ENSP00000466655.2:n.*1144_*1147dup
ENST00000593195.6:c.1697_1700dup	ENSP00000466073.1:n.1697_1700dup
ENST00000642541.1:c.1317_1320dup	ENSP00000493665.1:p.Asp441Ter
ENST00000681521.1:c.1365_1368dup	ENSP00000506037.1:p.Asp457Ter
ENST00000269197.9:c.1485_1488dup	ENSP00000269197.4:p.Asp497Ter
ENST00000592288.5:c.*609_*612dup	ENSP00000465053.1:n.*609_*612dup
NM_030632.1:c.1485_1488dup	NP_085135.1:p.Asp497Ter
XM_005258356.1:c.1488_1491dup	XP_005258413.1:p.Asp498Ter
XM_011526205.1:c.1461_1464dup	XP_011524507.1:p.Asp489Ter
XM_011526206.1:c.1407_1410dup	XP_011524508.1:p.Asp471Ter
XM_011526207.1:c.1407_1410dup	XP_011524509.1:p.Asp471Ter
XM_011526208.1:c.1368_1371dup	XP_011524510.1:p.Asp458Ter
XM_011526209.1:c.1317_1320dup	XP_011524511.1:p.Asp441Ter
XM_011526210.1:c.1317_1320dup	XP_011524512.1:p.Asp441Ter
XM_011526211.1:c.1317_1320dup	XP_011524513.1:p.Asp441Ter
XM_011526212.1:c.1317_1320dup	XP_011524514.1:p.Asp441Ter
XM_011526213.1:c.1317_1320dup	XP_011524515.1:p.Asp441Ter
XM_011526214.1:c.1317_1320dup	XP_011524516.1:p.Asp441Ter
NM_030632.2:c.1485_1488dup	NP_085135.1:p.Asp497Ter
XM_011526205.2:c.1461_1464dup	XP_011524507.1:p.Asp489Ter
XM_011526206.2:c.1407_1410dup	XP_011524508.1:p.Asp471Ter
XM_011526213.2:c.1317_1320dup	XP_011524515.1:p.Asp441Ter
XM_017026012.1:c.1407_1410dup	XP_016881501.1:p.Asp471Ter
XM_017026013.1:c.1317_1320dup	XP_016881502.1:p.Asp441Ter
XM_017026014.2:c.1317_1320dup	XP_016881503.1:p.Asp441Ter
XM_024451269.1:c.1317_1320dup	XP_024307037.1:p.Asp441Ter
NM_030632.3:c.1485_1488dup MANE Select	NP_085135.1:p.Asp497Ter