Canonical Allele Identifier: CA402176716

Gene: ASXL3

Linked Data

• MyVariant Identifiers: chr18:g.31319248C>A (hg19) ; chr18:g.33739284C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33739284C>A , CM000680.2:g.33739284C>A	GRCh38
NC_000018.9:g.31319248C>A , CM000680.1:g.31319248C>A	GRCh37
NC_000018.8:g.29573246C>A	NCBI36
NG_055244.1:g.165708C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.1883C>A	ENSP00000513003.1:p.Ser628Tyr
ENST00000269197.12:c.1880C>A MANE Select	ENSP00000269197.4:p.Ser627Tyr
ENST00000592288.6:c.*1004C>A	ENSP00000465053.1:n.*1004C>A
ENST00000592541.6:c.*1539C>A	ENSP00000466655.2:n.*1539C>A
ENST00000593195.6:c.2092C>A	ENSP00000466073.1:n.2092C>A
ENST00000642541.1:c.1712C>A	ENSP00000493665.1:p.Ser571Tyr
ENST00000681521.1:c.1760C>A	ENSP00000506037.1:p.Ser587Tyr
ENST00000269197.9:c.1880C>A	ENSP00000269197.4:p.Ser627Tyr
ENST00000592288.5:c.*1004C>A	ENSP00000465053.1:n.*1004C>A
NM_030632.1:c.1880C>A	NP_085135.1:p.Ser627Tyr
XM_005258356.1:c.1883C>A	XP_005258413.1:p.Ser628Tyr
XM_011526205.1:c.1856C>A	XP_011524507.1:p.Ser619Tyr
XM_011526206.1:c.1802C>A	XP_011524508.1:p.Ser601Tyr
XM_011526207.1:c.1802C>A	XP_011524509.1:p.Ser601Tyr
XM_011526208.1:c.1763C>A	XP_011524510.1:p.Ser588Tyr
XM_011526209.1:c.1712C>A	XP_011524511.1:p.Ser571Tyr
XM_011526210.1:c.1712C>A	XP_011524512.1:p.Ser571Tyr
XM_011526211.1:c.1712C>A	XP_011524513.1:p.Ser571Tyr
XM_011526212.1:c.1712C>A	XP_011524514.1:p.Ser571Tyr
XM_011526213.1:c.1712C>A	XP_011524515.1:p.Ser571Tyr
XM_011526214.1:c.1712C>A	XP_011524516.1:p.Ser571Tyr
NM_030632.2:c.1880C>A	NP_085135.1:p.Ser627Tyr
XM_011526205.2:c.1856C>A	XP_011524507.1:p.Ser619Tyr
XM_011526206.2:c.1802C>A	XP_011524508.1:p.Ser601Tyr
XM_011526213.2:c.1712C>A	XP_011524515.1:p.Ser571Tyr
XM_017026012.1:c.1802C>A	XP_016881501.1:p.Ser601Tyr
XM_017026013.1:c.1712C>A	XP_016881502.1:p.Ser571Tyr
XM_017026014.2:c.1712C>A	XP_016881503.1:p.Ser571Tyr
XM_024451269.1:c.1712C>A	XP_024307037.1:p.Ser571Tyr
NM_030632.3:c.1880C>A MANE Select	NP_085135.1:p.Ser627Tyr