Canonical Allele Identifier: CA402188678

Gene: ASXL3

Linked Data

• MyVariant Identifiers: chr18:g.31323712T>G (hg19) ; chr18:g.33743748T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33743748T>G , CM000680.2:g.33743748T>G	GRCh38
NC_000018.9:g.31323712T>G , CM000680.1:g.31323712T>G	GRCh37
NC_000018.8:g.29577710T>G	NCBI36
NG_055244.1:g.170172T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.3903T>G	ENSP00000513003.1:p.Ile1301Met
ENST00000269197.12:c.3900T>G MANE Select	ENSP00000269197.4:p.Ile1300Met
ENST00000681521.1:c.3780T>G	ENSP00000506037.1:p.Ile1260Met
ENST00000269197.9:c.3900T>G	ENSP00000269197.4:p.Ile1300Met
NM_030632.1:c.3900T>G	NP_085135.1:p.Ile1300Met
XM_005258356.1:c.3903T>G	XP_005258413.1:p.Ile1301Met
XM_011526205.1:c.3876T>G	XP_011524507.1:p.Ile1292Met
XM_011526206.1:c.3822T>G	XP_011524508.1:p.Ile1274Met
XM_011526207.1:c.3822T>G	XP_011524509.1:p.Ile1274Met
XM_011526208.1:c.3783T>G	XP_011524510.1:p.Ile1261Met
XM_011526209.1:c.3732T>G	XP_011524511.1:p.Ile1244Met
XM_011526210.1:c.3732T>G	XP_011524512.1:p.Ile1244Met
XM_011526211.1:c.3732T>G	XP_011524513.1:p.Ile1244Met
XM_011526212.1:c.3732T>G	XP_011524514.1:p.Ile1244Met
XM_011526213.1:c.3732T>G	XP_011524515.1:p.Ile1244Met
XM_011526214.1:c.3732T>G	XP_011524516.1:p.Ile1244Met
XM_011526215.1:c.864T>G	XP_011524517.1:p.Ile288Met
NM_030632.2:c.3900T>G	NP_085135.1:p.Ile1300Met
XM_011526205.2:c.3876T>G	XP_011524507.1:p.Ile1292Met
XM_011526206.2:c.3822T>G	XP_011524508.1:p.Ile1274Met
XM_011526213.2:c.3732T>G	XP_011524515.1:p.Ile1244Met
XM_017026012.1:c.3822T>G	XP_016881501.1:p.Ile1274Met
XM_017026013.1:c.3732T>G	XP_016881502.1:p.Ile1244Met
XM_017026014.2:c.3732T>G	XP_016881503.1:p.Ile1244Met
XM_024451269.1:c.3732T>G	XP_024307037.1:p.Ile1244Met
NM_030632.3:c.3900T>G MANE Select	NP_085135.1:p.Ile1300Met