Canonical Allele Identifier: CA402185199

Gene: ASXL3

Linked Data

• dbSNP Id: rs979454747
• gnomAD v2: 18-31323183-C-G
• gnomAD v3: 18-33743219-C-G
• gnomAD v4: 18-33743219-C-G
• COSMIC: COSM5429966 ; COSM5429967
• MyVariant Identifiers: chr18:g.31323183C>G (hg19) ; chr18:g.33743219C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33743219C>G , CM000680.2:g.33743219C>G	GRCh38
NC_000018.9:g.31323183C>G , CM000680.1:g.31323183C>G	GRCh37
NC_000018.8:g.29577181C>G	NCBI36
NG_055244.1:g.169643C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000696964.1:c.3374C>G	ENSP00000513003.1:p.Ser1125Cys
ENST00000269197.12:c.3371C>G MANE Select	ENSP00000269197.4:p.Ser1124Cys
ENST00000592288.6:c.*2495C>G	ENSP00000465053.1:n.*2495C>G
ENST00000592541.6:c.*3030C>G	ENSP00000466655.2:n.*3030C>G
ENST00000593195.6:c.3583C>G	ENSP00000466073.1:n.3583C>G
ENST00000642541.1:c.3203C>G	ENSP00000493665.1:p.Ser1068Cys
ENST00000681521.1:c.3251C>G	ENSP00000506037.1:p.Ser1084Cys
ENST00000269197.9:c.3371C>G	ENSP00000269197.4:p.Ser1124Cys
ENST00000592288.5:c.*2495C>G	ENSP00000465053.1:n.*2495C>G
NM_030632.1:c.3371C>G	NP_085135.1:p.Ser1124Cys
XM_005258356.1:c.3374C>G	XP_005258413.1:p.Ser1125Cys
XM_011526205.1:c.3347C>G	XP_011524507.1:p.Ser1116Cys
XM_011526206.1:c.3293C>G	XP_011524508.1:p.Ser1098Cys
XM_011526207.1:c.3293C>G	XP_011524509.1:p.Ser1098Cys
XM_011526208.1:c.3254C>G	XP_011524510.1:p.Ser1085Cys
XM_011526209.1:c.3203C>G	XP_011524511.1:p.Ser1068Cys
XM_011526210.1:c.3203C>G	XP_011524512.1:p.Ser1068Cys
XM_011526211.1:c.3203C>G	XP_011524513.1:p.Ser1068Cys
XM_011526212.1:c.3203C>G	XP_011524514.1:p.Ser1068Cys
XM_011526213.1:c.3203C>G	XP_011524515.1:p.Ser1068Cys
XM_011526214.1:c.3203C>G	XP_011524516.1:p.Ser1068Cys
XM_011526215.1:c.335C>G	XP_011524517.1:p.Ser112Cys
NM_030632.2:c.3371C>G	NP_085135.1:p.Ser1124Cys
XM_011526205.2:c.3347C>G	XP_011524507.1:p.Ser1116Cys
XM_011526206.2:c.3293C>G	XP_011524508.1:p.Ser1098Cys
XM_011526213.2:c.3203C>G	XP_011524515.1:p.Ser1068Cys
XM_017026012.1:c.3293C>G	XP_016881501.1:p.Ser1098Cys
XM_017026013.1:c.3203C>G	XP_016881502.1:p.Ser1068Cys
XM_017026014.2:c.3203C>G	XP_016881503.1:p.Ser1068Cys
XM_024451269.1:c.3203C>G	XP_024307037.1:p.Ser1068Cys
NM_030632.3:c.3371C>G MANE Select	NP_085135.1:p.Ser1124Cys