Canonical Allele Identifier: CA2360293784

Gene: ASXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436604A= , CM000682.2:g.32436604A=	GRCh38
NC_000020.10:g.31024407A= , CM000682.1:g.31024407A=	GRCh37
NC_000020.9:g.30488068A=	NCBI36
NG_027868.1:g.83261A= , LRG_630:g.83261A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3892A= MANE Select	ENSP00000364839.4:p.Thr1298=
ENST00000646985.1:c.3709A=	ENSP00000495053.1:p.Thr1237=
ENST00000647223.1:n.6245A=
ENST00000651418.1:c.1870-1826A=	ENSP00000499150.1:n.1870-1826A=
ENST00000306058.9:c.3877A=	ENSP00000305119.5:p.Thr1293=
ENST00000375687.8:c.3892A=	ENSP00000364839.4:p.Thr1298=
ENST00000613218.4:c.3892A=	ENSP00000480487.1:p.Thr1298=
ENST00000620121.4:c.3892A=	ENSP00000481978.1:p.Thr1298=
NM_015338.5:c.3892A= , LRG_630t1:c.3892A=	NP_056153.2:p.Thr1298=
XM_006723727.2:c.3889A=	XP_006723790.1:p.Thr1297=
XM_006723728.2:c.3862A=	XP_006723791.1:p.Thr1288=
XM_006723730.2:c.3808A=	XP_006723793.1:p.Thr1270=
XM_006723732.2:c.3709A=	XP_006723795.1:p.Thr1237=
XM_006723733.1:c.3208A=	XP_006723796.1:p.Thr1070=
XM_011528647.1:c.4156A=	XP_011526949.1:p.Thr1386=
XM_011528648.1:c.4153A=	XP_011526950.1:p.Thr1385=
XM_011528649.1:c.4072A=	XP_011526951.1:p.Thr1358=
XM_011528650.1:c.4003A=	XP_011526952.1:p.Thr1335=
XM_011528651.1:c.3871A=	XP_011526953.1:p.Thr1291=
XM_011528652.1:c.3808A=	XP_011526954.1:p.Thr1270=
NM_001363734.1:c.3709A=	NP_001350663.1:p.Thr1237=
XM_006723727.3:c.3889A=	XP_006723790.1:p.Thr1297=
XM_006723728.3:c.3862A=	XP_006723791.1:p.Thr1288=
XM_006723730.4:c.3808A=	XP_006723793.1:p.Thr1270=
XM_011528648.3:c.4153A=	XP_011526950.1:p.Thr1385=
XM_011528652.2:c.3808A=	XP_011526954.1:p.Thr1270=
XM_017027704.1:c.3808A=	XP_016883193.1:p.Thr1270=
XM_017027705.1:c.3808A=	XP_016883194.1:p.Thr1270=
XM_017027706.1:c.3739A=	XP_016883195.1:p.Thr1247=
NM_015338.6:c.3892A= MANE Select	NP_056153.2:p.Thr1298=