Canonical Allele Identifier: CA402175408

Gene: ASXL3

Linked Data

• MyVariant Identifiers: chr18:g.31318827C>G (hg19) ; chr18:g.33738863C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33738863C>G , CM000680.2:g.33738863C>G	GRCh38
NC_000018.9:g.31318827C>G , CM000680.1:g.31318827C>G	GRCh37
NC_000018.8:g.29572825C>G	NCBI36
NG_055244.1:g.165287C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.1462C>G	ENSP00000513003.1:p.His488Asp
ENST00000269197.12:c.1459C>G MANE Select	ENSP00000269197.4:p.His487Asp
ENST00000592288.6:c.*583C>G	ENSP00000465053.1:n.*583C>G
ENST00000592541.6:c.*1118C>G	ENSP00000466655.2:n.*1118C>G
ENST00000593195.6:c.1671C>G	ENSP00000466073.1:n.1671C>G
ENST00000642541.1:c.1291C>G	ENSP00000493665.1:p.His431Asp
ENST00000681521.1:c.1339C>G	ENSP00000506037.1:p.His447Asp
ENST00000269197.9:c.1459C>G	ENSP00000269197.4:p.His487Asp
ENST00000592288.5:c.*583C>G	ENSP00000465053.1:n.*583C>G
NM_030632.1:c.1459C>G	NP_085135.1:p.His487Asp
XM_005258356.1:c.1462C>G	XP_005258413.1:p.His488Asp
XM_011526205.1:c.1435C>G	XP_011524507.1:p.His479Asp
XM_011526206.1:c.1381C>G	XP_011524508.1:p.His461Asp
XM_011526207.1:c.1381C>G	XP_011524509.1:p.His461Asp
XM_011526208.1:c.1342C>G	XP_011524510.1:p.His448Asp
XM_011526209.1:c.1291C>G	XP_011524511.1:p.His431Asp
XM_011526210.1:c.1291C>G	XP_011524512.1:p.His431Asp
XM_011526211.1:c.1291C>G	XP_011524513.1:p.His431Asp
XM_011526212.1:c.1291C>G	XP_011524514.1:p.His431Asp
XM_011526213.1:c.1291C>G	XP_011524515.1:p.His431Asp
XM_011526214.1:c.1291C>G	XP_011524516.1:p.His431Asp
NM_030632.2:c.1459C>G	NP_085135.1:p.His487Asp
XM_011526205.2:c.1435C>G	XP_011524507.1:p.His479Asp
XM_011526206.2:c.1381C>G	XP_011524508.1:p.His461Asp
XM_011526213.2:c.1291C>G	XP_011524515.1:p.His431Asp
XM_017026012.1:c.1381C>G	XP_016881501.1:p.His461Asp
XM_017026013.1:c.1291C>G	XP_016881502.1:p.His431Asp
XM_017026014.2:c.1291C>G	XP_016881503.1:p.His431Asp
XM_024451269.1:c.1291C>G	XP_024307037.1:p.His431Asp
NM_030632.3:c.1459C>G MANE Select	NP_085135.1:p.His487Asp