Canonical Allele Identifier: CA8933758

Gene: ASXL3

Linked Data

• dbSNP Id: rs748942696
• ExAC: 18:31318841 A / G
• gnomAD v2: 18-31318841-A-G
• gnomAD v4: 18-33738877-A-G
• MyVariant Identifiers: chr18:g.31318841A>G (hg19) ; chr18:g.33738877A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33738877A>G , CM000680.2:g.33738877A>G	GRCh38
NC_000018.9:g.31318841A>G , CM000680.1:g.31318841A>G	GRCh37
NC_000018.8:g.29572839A>G	NCBI36
NG_055244.1:g.165301A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.1476A>G	ENSP00000513003.1:p.Gln492=
ENST00000269197.12:c.1473A>G MANE Select	ENSP00000269197.4:p.Gln491=
ENST00000592288.6:c.*597A>G	ENSP00000465053.1:n.*597A>G
ENST00000592541.6:c.*1132A>G	ENSP00000466655.2:n.*1132A>G
ENST00000593195.6:c.1685A>G	ENSP00000466073.1:n.1685A>G
ENST00000642541.1:c.1305A>G	ENSP00000493665.1:p.Gln435=
ENST00000681521.1:c.1353A>G	ENSP00000506037.1:p.Gln451=
ENST00000269197.9:c.1473A>G	ENSP00000269197.4:p.Gln491=
ENST00000592288.5:c.*597A>G	ENSP00000465053.1:n.*597A>G
NM_030632.1:c.1473A>G	NP_085135.1:p.Gln491=
XM_005258356.1:c.1476A>G	XP_005258413.1:p.Gln492=
XM_011526205.1:c.1449A>G	XP_011524507.1:p.Gln483=
XM_011526206.1:c.1395A>G	XP_011524508.1:p.Gln465=
XM_011526207.1:c.1395A>G	XP_011524509.1:p.Gln465=
XM_011526208.1:c.1356A>G	XP_011524510.1:p.Gln452=
XM_011526209.1:c.1305A>G	XP_011524511.1:p.Gln435=
XM_011526210.1:c.1305A>G	XP_011524512.1:p.Gln435=
XM_011526211.1:c.1305A>G	XP_011524513.1:p.Gln435=
XM_011526212.1:c.1305A>G	XP_011524514.1:p.Gln435=
XM_011526213.1:c.1305A>G	XP_011524515.1:p.Gln435=
XM_011526214.1:c.1305A>G	XP_011524516.1:p.Gln435=
NM_030632.2:c.1473A>G	NP_085135.1:p.Gln491=
XM_011526205.2:c.1449A>G	XP_011524507.1:p.Gln483=
XM_011526206.2:c.1395A>G	XP_011524508.1:p.Gln465=
XM_011526213.2:c.1305A>G	XP_011524515.1:p.Gln435=
XM_017026012.1:c.1395A>G	XP_016881501.1:p.Gln465=
XM_017026013.1:c.1305A>G	XP_016881502.1:p.Gln435=
XM_017026014.2:c.1305A>G	XP_016881503.1:p.Gln435=
XM_024451269.1:c.1305A>G	XP_024307037.1:p.Gln435=
NM_030632.3:c.1473A>G MANE Select	NP_085135.1:p.Gln491=