Canonical Allele Identifier: CA1139666035

Gene: ASXL3

Linked Data

• ClinVar Variation Id: 984845
• ClinVar RCV Id: RCV001265363
• dbSNP Id: rs2067717913

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33744012dup , CM000680.2:g.33744012dup	GRCh38
NC_000018.9:g.31323976dup , CM000680.1:g.31323976dup	GRCh37
NC_000018.8:g.29577974dup	NCBI36
NG_055244.1:g.170436dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.4167dup	ENSP00000513003.1:p.Thr1390TyrfsTer11
ENST00000269197.12:c.4164dup MANE Select	ENSP00000269197.4:p.Thr1389TyrfsTer11
ENST00000681521.1:c.4044dup	ENSP00000506037.1:p.Thr1349TyrfsTer11
ENST00000269197.9:c.4164dup	ENSP00000269197.4:p.Thr1389TyrfsTer11
NM_030632.1:c.4164dup	NP_085135.1:p.Thr1389TyrfsTer11
XM_005258356.1:c.4167dup	XP_005258413.1:p.Thr1390TyrfsTer11
XM_011526205.1:c.4140dup	XP_011524507.1:p.Thr1381TyrfsTer11
XM_011526206.1:c.4086dup	XP_011524508.1:p.Thr1363TyrfsTer11
XM_011526207.1:c.4086dup	XP_011524509.1:p.Thr1363TyrfsTer11
XM_011526208.1:c.4047dup	XP_011524510.1:p.Thr1350TyrfsTer11
XM_011526209.1:c.3996dup	XP_011524511.1:p.Thr1333TyrfsTer11
XM_011526210.1:c.3996dup	XP_011524512.1:p.Thr1333TyrfsTer11
XM_011526211.1:c.3996dup	XP_011524513.1:p.Thr1333TyrfsTer11
XM_011526212.1:c.3996dup	XP_011524514.1:p.Thr1333TyrfsTer11
XM_011526213.1:c.3996dup	XP_011524515.1:p.Thr1333TyrfsTer11
XM_011526214.1:c.3996dup	XP_011524516.1:p.Thr1333TyrfsTer11
XM_011526215.1:c.1128dup	XP_011524517.1:p.Thr377TyrfsTer11
NM_030632.2:c.4164dup	NP_085135.1:p.Thr1389TyrfsTer11
XM_011526205.2:c.4140dup	XP_011524507.1:p.Thr1381TyrfsTer11
XM_011526206.2:c.4086dup	XP_011524508.1:p.Thr1363TyrfsTer11
XM_011526213.2:c.3996dup	XP_011524515.1:p.Thr1333TyrfsTer11
XM_017026012.1:c.4086dup	XP_016881501.1:p.Thr1363TyrfsTer11
XM_017026013.1:c.3996dup	XP_016881502.1:p.Thr1333TyrfsTer11
XM_017026014.2:c.3996dup	XP_016881503.1:p.Thr1333TyrfsTer11
XM_024451269.1:c.3996dup	XP_024307037.1:p.Thr1333TyrfsTer11
NM_030632.3:c.4164dup MANE Select	NP_085135.1:p.Thr1389TyrfsTer11