Canonical Allele Identifier: CA2360293548

Gene: ASXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436134A= , CM000682.2:g.32436134A=	GRCh38
NC_000020.10:g.31023937A= , CM000682.1:g.31023937A=	GRCh37
NC_000020.9:g.30487598A=	NCBI36
NG_027868.1:g.82791A= , LRG_630:g.82791A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3422A= MANE Select	ENSP00000364839.4:p.Asp1141=
ENST00000646985.1:c.3239A=	ENSP00000495053.1:p.Asp1080=
ENST00000647223.1:n.5775A=
ENST00000651418.1:c.1869+1553A=	ENSP00000499150.1:n.1869+1553A=
ENST00000306058.9:c.3407A=	ENSP00000305119.5:p.Asp1136=
ENST00000375687.8:c.3422A=	ENSP00000364839.4:p.Asp1141=
ENST00000613218.4:c.3422A=	ENSP00000480487.1:p.Asp1141=
ENST00000620121.4:c.3422A=	ENSP00000481978.1:p.Asp1141=
NM_015338.5:c.3422A= , LRG_630t1:c.3422A=	NP_056153.2:p.Asp1141=
XM_006723727.2:c.3419A=	XP_006723790.1:p.Asp1140=
XM_006723728.2:c.3392A=	XP_006723791.1:p.Asp1131=
XM_006723730.2:c.3338A=	XP_006723793.1:p.Asp1113=
XM_006723732.2:c.3239A=	XP_006723795.1:p.Asp1080=
XM_006723733.1:c.2738A=	XP_006723796.1:p.Asp913=
XM_011528647.1:c.3686A=	XP_011526949.1:p.Asp1229=
XM_011528648.1:c.3683A=	XP_011526950.1:p.Asp1228=
XM_011528649.1:c.3602A=	XP_011526951.1:p.Asp1201=
XM_011528650.1:c.3533A=	XP_011526952.1:p.Asp1178=
XM_011528651.1:c.3401A=	XP_011526953.1:p.Asp1134=
XM_011528652.1:c.3338A=	XP_011526954.1:p.Asp1113=
NM_001363734.1:c.3239A=	NP_001350663.1:p.Asp1080=
XM_006723727.3:c.3419A=	XP_006723790.1:p.Asp1140=
XM_006723728.3:c.3392A=	XP_006723791.1:p.Asp1131=
XM_006723730.4:c.3338A=	XP_006723793.1:p.Asp1113=
XM_011528648.3:c.3683A=	XP_011526950.1:p.Asp1228=
XM_011528652.2:c.3338A=	XP_011526954.1:p.Asp1113=
XM_017027704.1:c.3338A=	XP_016883193.1:p.Asp1113=
XM_017027705.1:c.3338A=	XP_016883194.1:p.Asp1113=
XM_017027706.1:c.3269A=	XP_016883195.1:p.Asp1090=
NM_015338.6:c.3422A= MANE Select	NP_056153.2:p.Asp1141=