Canonical Allele Identifier: CA2360293862

Gene: ASXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436775G= , CM000682.2:g.32436775G=	GRCh38
NC_000020.10:g.31024578G= , CM000682.1:g.31024578G=	GRCh37
NC_000020.9:g.30488239G=	NCBI36
NG_027868.1:g.83432G= , LRG_630:g.83432G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.4063G= MANE Select	ENSP00000364839.4:p.Asp1355=
ENST00000646985.1:c.3880G=	ENSP00000495053.1:p.Asp1294=
ENST00000647223.1:n.6416G=
ENST00000651418.1:c.1870-1655G=	ENSP00000499150.1:n.1870-1655G=
ENST00000306058.9:c.4048G=	ENSP00000305119.5:p.Asp1350=
ENST00000375687.8:c.4063G=	ENSP00000364839.4:p.Asp1355=
ENST00000613218.4:c.4063G=	ENSP00000480487.1:p.Asp1355=
ENST00000620121.4:c.4063G=	ENSP00000481978.1:p.Asp1355=
NM_015338.5:c.4063G= , LRG_630t1:c.4063G=	NP_056153.2:p.Asp1355=
XM_006723727.2:c.4060G=	XP_006723790.1:p.Asp1354=
XM_006723728.2:c.4033G=	XP_006723791.1:p.Asp1345=
XM_006723730.2:c.3979G=	XP_006723793.1:p.Asp1327=
XM_006723732.2:c.3880G=	XP_006723795.1:p.Asp1294=
XM_006723733.1:c.3379G=	XP_006723796.1:p.Asp1127=
XM_011528647.1:c.4327G=	XP_011526949.1:p.Asp1443=
XM_011528648.1:c.4324G=	XP_011526950.1:p.Asp1442=
XM_011528649.1:c.4243G=	XP_011526951.1:p.Asp1415=
XM_011528650.1:c.4174G=	XP_011526952.1:p.Asp1392=
XM_011528651.1:c.4042G=	XP_011526953.1:p.Asp1348=
XM_011528652.1:c.3979G=	XP_011526954.1:p.Asp1327=
NM_001363734.1:c.3880G=	NP_001350663.1:p.Asp1294=
XM_006723727.3:c.4060G=	XP_006723790.1:p.Asp1354=
XM_006723728.3:c.4033G=	XP_006723791.1:p.Asp1345=
XM_006723730.4:c.3979G=	XP_006723793.1:p.Asp1327=
XM_011528648.3:c.4324G=	XP_011526950.1:p.Asp1442=
XM_011528652.2:c.3979G=	XP_011526954.1:p.Asp1327=
XM_017027704.1:c.3979G=	XP_016883193.1:p.Asp1327=
XM_017027705.1:c.3979G=	XP_016883194.1:p.Asp1327=
XM_017027706.1:c.3910G=	XP_016883195.1:p.Asp1304=
NM_015338.6:c.4063G= MANE Select	NP_056153.2:p.Asp1355=