Canonical Allele Identifier: CA2360293665

Gene: ASXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436362C= , CM000682.2:g.32436362C=	GRCh38
NC_000020.10:g.31024165C= , CM000682.1:g.31024165C=	GRCh37
NC_000020.9:g.30487826C=	NCBI36
NG_027868.1:g.83019C= , LRG_630:g.83019C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3650C= MANE Select	ENSP00000364839.4:p.Thr1217=
ENST00000646985.1:c.3467C=	ENSP00000495053.1:p.Thr1156=
ENST00000647223.1:n.6003C=
ENST00000651418.1:c.1869+1781C=	ENSP00000499150.1:n.1869+1781C=
ENST00000306058.9:c.3635C=	ENSP00000305119.5:p.Thr1212=
ENST00000375687.8:c.3650C=	ENSP00000364839.4:p.Thr1217=
ENST00000613218.4:c.3650C=	ENSP00000480487.1:p.Thr1217=
ENST00000620121.4:c.3650C=	ENSP00000481978.1:p.Thr1217=
NM_015338.5:c.3650C= , LRG_630t1:c.3650C=	NP_056153.2:p.Thr1217=
XM_006723727.2:c.3647C=	XP_006723790.1:p.Thr1216=
XM_006723728.2:c.3620C=	XP_006723791.1:p.Thr1207=
XM_006723730.2:c.3566C=	XP_006723793.1:p.Thr1189=
XM_006723732.2:c.3467C=	XP_006723795.1:p.Thr1156=
XM_006723733.1:c.2966C=	XP_006723796.1:p.Thr989=
XM_011528647.1:c.3914C=	XP_011526949.1:p.Thr1305=
XM_011528648.1:c.3911C=	XP_011526950.1:p.Thr1304=
XM_011528649.1:c.3830C=	XP_011526951.1:p.Thr1277=
XM_011528650.1:c.3761C=	XP_011526952.1:p.Thr1254=
XM_011528651.1:c.3629C=	XP_011526953.1:p.Thr1210=
XM_011528652.1:c.3566C=	XP_011526954.1:p.Thr1189=
NM_001363734.1:c.3467C=	NP_001350663.1:p.Thr1156=
XM_006723727.3:c.3647C=	XP_006723790.1:p.Thr1216=
XM_006723728.3:c.3620C=	XP_006723791.1:p.Thr1207=
XM_006723730.4:c.3566C=	XP_006723793.1:p.Thr1189=
XM_011528648.3:c.3911C=	XP_011526950.1:p.Thr1304=
XM_011528652.2:c.3566C=	XP_011526954.1:p.Thr1189=
XM_017027704.1:c.3566C=	XP_016883193.1:p.Thr1189=
XM_017027705.1:c.3566C=	XP_016883194.1:p.Thr1189=
XM_017027706.1:c.3497C=	XP_016883195.1:p.Thr1166=
NM_015338.6:c.3650C= MANE Select	NP_056153.2:p.Thr1217=