Canonical Allele Identifier: CA2360293861

Gene: ASXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436772G= , CM000682.2:g.32436772G=	GRCh38
NC_000020.10:g.31024575G= , CM000682.1:g.31024575G=	GRCh37
NC_000020.9:g.30488236G=	NCBI36
NG_027868.1:g.83429G= , LRG_630:g.83429G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.4060G= MANE Select	ENSP00000364839.4:p.Glu1354=
ENST00000646985.1:c.3877G=	ENSP00000495053.1:p.Glu1293=
ENST00000647223.1:n.6413G=
ENST00000651418.1:c.1870-1658G=	ENSP00000499150.1:n.1870-1658G=
ENST00000306058.9:c.4045G=	ENSP00000305119.5:p.Glu1349=
ENST00000375687.8:c.4060G=	ENSP00000364839.4:p.Glu1354=
ENST00000613218.4:c.4060G=	ENSP00000480487.1:p.Glu1354=
ENST00000620121.4:c.4060G=	ENSP00000481978.1:p.Glu1354=
NM_015338.5:c.4060G= , LRG_630t1:c.4060G=	NP_056153.2:p.Glu1354=
XM_006723727.2:c.4057G=	XP_006723790.1:p.Glu1353=
XM_006723728.2:c.4030G=	XP_006723791.1:p.Glu1344=
XM_006723730.2:c.3976G=	XP_006723793.1:p.Glu1326=
XM_006723732.2:c.3877G=	XP_006723795.1:p.Glu1293=
XM_006723733.1:c.3376G=	XP_006723796.1:p.Glu1126=
XM_011528647.1:c.4324G=	XP_011526949.1:p.Glu1442=
XM_011528648.1:c.4321G=	XP_011526950.1:p.Glu1441=
XM_011528649.1:c.4240G=	XP_011526951.1:p.Glu1414=
XM_011528650.1:c.4171G=	XP_011526952.1:p.Glu1391=
XM_011528651.1:c.4039G=	XP_011526953.1:p.Glu1347=
XM_011528652.1:c.3976G=	XP_011526954.1:p.Glu1326=
NM_001363734.1:c.3877G=	NP_001350663.1:p.Glu1293=
XM_006723727.3:c.4057G=	XP_006723790.1:p.Glu1353=
XM_006723728.3:c.4030G=	XP_006723791.1:p.Glu1344=
XM_006723730.4:c.3976G=	XP_006723793.1:p.Glu1326=
XM_011528648.3:c.4321G=	XP_011526950.1:p.Glu1441=
XM_011528652.2:c.3976G=	XP_011526954.1:p.Glu1326=
XM_017027704.1:c.3976G=	XP_016883193.1:p.Glu1326=
XM_017027705.1:c.3976G=	XP_016883194.1:p.Glu1326=
XM_017027706.1:c.3907G=	XP_016883195.1:p.Glu1303=
NM_015338.6:c.4060G= MANE Select	NP_056153.2:p.Glu1354=