Canonical Allele Identifier: CA2360293449

Gene: ASXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32435900A= , CM000682.2:g.32435900A=	GRCh38
NC_000020.10:g.31023703A= , CM000682.1:g.31023703A=	GRCh37
NC_000020.9:g.30487364A=	NCBI36
NG_027868.1:g.82557A= , LRG_630:g.82557A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3188A= MANE Select	ENSP00000364839.4:p.Gln1063=
ENST00000646985.1:c.3005A=	ENSP00000495053.1:p.Gln1002=
ENST00000647223.1:n.5541A=
ENST00000651418.1:c.1869+1319A=	ENSP00000499150.1:n.1869+1319A=
ENST00000306058.9:c.3173A=	ENSP00000305119.5:p.Gln1058=
ENST00000375687.8:c.3188A=	ENSP00000364839.4:p.Gln1063=
ENST00000613218.4:c.3188A=	ENSP00000480487.1:p.Gln1063=
ENST00000620121.4:c.3188A=	ENSP00000481978.1:p.Gln1063=
NM_015338.5:c.3188A= , LRG_630t1:c.3188A=	NP_056153.2:p.Gln1063=
XM_006723727.2:c.3185A=	XP_006723790.1:p.Gln1062=
XM_006723728.2:c.3158A=	XP_006723791.1:p.Gln1053=
XM_006723730.2:c.3104A=	XP_006723793.1:p.Gln1035=
XM_006723732.2:c.3005A=	XP_006723795.1:p.Gln1002=
XM_006723733.1:c.2504A=	XP_006723796.1:p.Gln835=
XM_011528647.1:c.3452A=	XP_011526949.1:p.Gln1151=
XM_011528648.1:c.3449A=	XP_011526950.1:p.Gln1150=
XM_011528649.1:c.3368A=	XP_011526951.1:p.Gln1123=
XM_011528650.1:c.3299A=	XP_011526952.1:p.Gln1100=
XM_011528651.1:c.3167A=	XP_011526953.1:p.Gln1056=
XM_011528652.1:c.3104A=	XP_011526954.1:p.Gln1035=
NM_001363734.1:c.3005A=	NP_001350663.1:p.Gln1002=
XM_006723727.3:c.3185A=	XP_006723790.1:p.Gln1062=
XM_006723728.3:c.3158A=	XP_006723791.1:p.Gln1053=
XM_006723730.4:c.3104A=	XP_006723793.1:p.Gln1035=
XM_011528648.3:c.3449A=	XP_011526950.1:p.Gln1150=
XM_011528652.2:c.3104A=	XP_011526954.1:p.Gln1035=
XM_017027704.1:c.3104A=	XP_016883193.1:p.Gln1035=
XM_017027705.1:c.3104A=	XP_016883194.1:p.Gln1035=
XM_017027706.1:c.3035A=	XP_016883195.1:p.Gln1012=
NM_015338.6:c.3188A= MANE Select	NP_056153.2:p.Gln1063=