Canonical Allele Identifier: CA2294855724

Gene: ASXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33738881_33738883delinsGCA , CM000680.2:g.33738881_33738883delinsGCA	GRCh38
NC_000018.9:g.31318845_31318847delinsGCA , CM000680.1:g.31318845_31318847delinsGCA	GRCh37
NC_000018.8:g.29572843_29572845delinsGCA	NCBI36
NG_055244.1:g.165305_165307delinsGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.1480_1482delinsGCA	ENSP00000513003.1:p.Ala494=
ENST00000269197.12:c.1477_1479delinsGCA MANE Select	ENSP00000269197.4:p.Ala493=
ENST00000592288.6:c.*601_*603delinsGCA	ENSP00000465053.1:n.*601_*603delinsGCA
ENST00000592541.6:c.*1136_*1138delinsGCA	ENSP00000466655.2:n.*1136_*1138delinsGCA
ENST00000593195.6:c.1689_1691delinsGCA	ENSP00000466073.1:n.1689_1691delinsGCA
ENST00000642541.1:c.1309_1311delinsGCA	ENSP00000493665.1:p.Ala437=
ENST00000681521.1:c.1357_1359delinsGCA	ENSP00000506037.1:p.Ala453=
ENST00000269197.9:c.1477_1479delinsGCA	ENSP00000269197.4:p.Ala493=
ENST00000592288.5:c.*601_*603delinsGCA	ENSP00000465053.1:n.*601_*603delinsGCA
NM_030632.1:c.1477_1479delinsGCA	NP_085135.1:p.Ala493=
XM_005258356.1:c.1480_1482delinsGCA	XP_005258413.1:p.Ala494=
XM_011526205.1:c.1453_1455delinsGCA	XP_011524507.1:p.Ala485=
XM_011526206.1:c.1399_1401delinsGCA	XP_011524508.1:p.Ala467=
XM_011526207.1:c.1399_1401delinsGCA	XP_011524509.1:p.Ala467=
XM_011526208.1:c.1360_1362delinsGCA	XP_011524510.1:p.Ala454=
XM_011526209.1:c.1309_1311delinsGCA	XP_011524511.1:p.Ala437=
XM_011526210.1:c.1309_1311delinsGCA	XP_011524512.1:p.Ala437=
XM_011526211.1:c.1309_1311delinsGCA	XP_011524513.1:p.Ala437=
XM_011526212.1:c.1309_1311delinsGCA	XP_011524514.1:p.Ala437=
XM_011526213.1:c.1309_1311delinsGCA	XP_011524515.1:p.Ala437=
XM_011526214.1:c.1309_1311delinsGCA	XP_011524516.1:p.Ala437=
NM_030632.2:c.1477_1479delinsGCA	NP_085135.1:p.Ala493=
XM_011526205.2:c.1453_1455delinsGCA	XP_011524507.1:p.Ala485=
XM_011526206.2:c.1399_1401delinsGCA	XP_011524508.1:p.Ala467=
XM_011526213.2:c.1309_1311delinsGCA	XP_011524515.1:p.Ala437=
XM_017026012.1:c.1399_1401delinsGCA	XP_016881501.1:p.Ala467=
XM_017026013.1:c.1309_1311delinsGCA	XP_016881502.1:p.Ala437=
XM_017026014.2:c.1309_1311delinsGCA	XP_016881503.1:p.Ala437=
XM_024451269.1:c.1309_1311delinsGCA	XP_024307037.1:p.Ala437=
NM_030632.3:c.1477_1479delinsGCA MANE Select	NP_085135.1:p.Ala493=