Canonical Allele Identifier: CA2360293496

Gene: ASXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436022A= , CM000682.2:g.32436022A=	GRCh38
NC_000020.10:g.31023825A= , CM000682.1:g.31023825A=	GRCh37
NC_000020.9:g.30487486A=	NCBI36
NG_027868.1:g.82679A= , LRG_630:g.82679A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3310A= MANE Select	ENSP00000364839.4:p.Thr1104=
ENST00000646985.1:c.3127A=	ENSP00000495053.1:p.Thr1043=
ENST00000647223.1:n.5663A=
ENST00000651418.1:c.1869+1441A=	ENSP00000499150.1:n.1869+1441A=
ENST00000306058.9:c.3295A=	ENSP00000305119.5:p.Thr1099=
ENST00000375687.8:c.3310A=	ENSP00000364839.4:p.Thr1104=
ENST00000613218.4:c.3310A=	ENSP00000480487.1:p.Thr1104=
ENST00000620121.4:c.3310A=	ENSP00000481978.1:p.Thr1104=
NM_015338.5:c.3310A= , LRG_630t1:c.3310A=	NP_056153.2:p.Thr1104=
XM_006723727.2:c.3307A=	XP_006723790.1:p.Thr1103=
XM_006723728.2:c.3280A=	XP_006723791.1:p.Thr1094=
XM_006723730.2:c.3226A=	XP_006723793.1:p.Thr1076=
XM_006723732.2:c.3127A=	XP_006723795.1:p.Thr1043=
XM_006723733.1:c.2626A=	XP_006723796.1:p.Thr876=
XM_011528647.1:c.3574A=	XP_011526949.1:p.Thr1192=
XM_011528648.1:c.3571A=	XP_011526950.1:p.Thr1191=
XM_011528649.1:c.3490A=	XP_011526951.1:p.Thr1164=
XM_011528650.1:c.3421A=	XP_011526952.1:p.Thr1141=
XM_011528651.1:c.3289A=	XP_011526953.1:p.Thr1097=
XM_011528652.1:c.3226A=	XP_011526954.1:p.Thr1076=
NM_001363734.1:c.3127A=	NP_001350663.1:p.Thr1043=
XM_006723727.3:c.3307A=	XP_006723790.1:p.Thr1103=
XM_006723728.3:c.3280A=	XP_006723791.1:p.Thr1094=
XM_006723730.4:c.3226A=	XP_006723793.1:p.Thr1076=
XM_011528648.3:c.3571A=	XP_011526950.1:p.Thr1191=
XM_011528652.2:c.3226A=	XP_011526954.1:p.Thr1076=
XM_017027704.1:c.3226A=	XP_016883193.1:p.Thr1076=
XM_017027705.1:c.3226A=	XP_016883194.1:p.Thr1076=
XM_017027706.1:c.3157A=	XP_016883195.1:p.Thr1053=
NM_015338.6:c.3310A= MANE Select	NP_056153.2:p.Thr1104=