Canonical Allele Identifier: CA402184758

Gene: ASXL3

Linked Data

• MyVariant Identifiers: chr18:g.31322994C>G (hg19) ; chr18:g.33743030C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33743030C>G , CM000680.2:g.33743030C>G	GRCh38
NC_000018.9:g.31322994C>G , CM000680.1:g.31322994C>G	GRCh37
NC_000018.8:g.29576992C>G	NCBI36
NG_055244.1:g.169454C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000696964.1:c.3185C>G	ENSP00000513003.1:p.Ala1062Gly
ENST00000269197.12:c.3182C>G MANE Select	ENSP00000269197.4:p.Ala1061Gly
ENST00000592288.6:c.*2306C>G	ENSP00000465053.1:n.*2306C>G
ENST00000592541.6:c.*2841C>G	ENSP00000466655.2:n.*2841C>G
ENST00000593195.6:c.3394C>G	ENSP00000466073.1:n.3394C>G
ENST00000642541.1:c.3014C>G	ENSP00000493665.1:p.Ala1005Gly
ENST00000681521.1:c.3062C>G	ENSP00000506037.1:p.Ala1021Gly
ENST00000269197.9:c.3182C>G	ENSP00000269197.4:p.Ala1061Gly
ENST00000592288.5:c.*2306C>G	ENSP00000465053.1:n.*2306C>G
NM_030632.1:c.3182C>G	NP_085135.1:p.Ala1061Gly
XM_005258356.1:c.3185C>G	XP_005258413.1:p.Ala1062Gly
XM_011526205.1:c.3158C>G	XP_011524507.1:p.Ala1053Gly
XM_011526206.1:c.3104C>G	XP_011524508.1:p.Ala1035Gly
XM_011526207.1:c.3104C>G	XP_011524509.1:p.Ala1035Gly
XM_011526208.1:c.3065C>G	XP_011524510.1:p.Ala1022Gly
XM_011526209.1:c.3014C>G	XP_011524511.1:p.Ala1005Gly
XM_011526210.1:c.3014C>G	XP_011524512.1:p.Ala1005Gly
XM_011526211.1:c.3014C>G	XP_011524513.1:p.Ala1005Gly
XM_011526212.1:c.3014C>G	XP_011524514.1:p.Ala1005Gly
XM_011526213.1:c.3014C>G	XP_011524515.1:p.Ala1005Gly
XM_011526214.1:c.3014C>G	XP_011524516.1:p.Ala1005Gly
XM_011526215.1:c.146C>G	XP_011524517.1:p.Ala49Gly
NM_030632.2:c.3182C>G	NP_085135.1:p.Ala1061Gly
XM_011526205.2:c.3158C>G	XP_011524507.1:p.Ala1053Gly
XM_011526206.2:c.3104C>G	XP_011524508.1:p.Ala1035Gly
XM_011526213.2:c.3014C>G	XP_011524515.1:p.Ala1005Gly
XM_017026012.1:c.3104C>G	XP_016881501.1:p.Ala1035Gly
XM_017026013.1:c.3014C>G	XP_016881502.1:p.Ala1005Gly
XM_017026014.2:c.3014C>G	XP_016881503.1:p.Ala1005Gly
XM_024451269.1:c.3014C>G	XP_024307037.1:p.Ala1005Gly
NM_030632.3:c.3182C>G MANE Select	NP_085135.1:p.Ala1061Gly