Canonical Allele Identifier: CA2360293534

Gene: ASXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436109T= , CM000682.2:g.32436109T=	GRCh38
NC_000020.10:g.31023912T= , CM000682.1:g.31023912T=	GRCh37
NC_000020.9:g.30487573T=	NCBI36
NG_027868.1:g.82766T= , LRG_630:g.82766T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3397T= MANE Select	ENSP00000364839.4:p.Ser1133=
ENST00000646985.1:c.3214T=	ENSP00000495053.1:p.Ser1072=
ENST00000647223.1:n.5750T=
ENST00000651418.1:c.1869+1528T=	ENSP00000499150.1:n.1869+1528T=
ENST00000306058.9:c.3382T=	ENSP00000305119.5:p.Ser1128=
ENST00000375687.8:c.3397T=	ENSP00000364839.4:p.Ser1133=
ENST00000613218.4:c.3397T=	ENSP00000480487.1:p.Ser1133=
ENST00000620121.4:c.3397T=	ENSP00000481978.1:p.Ser1133=
NM_015338.5:c.3397T= , LRG_630t1:c.3397T=	NP_056153.2:p.Ser1133=
XM_006723727.2:c.3394T=	XP_006723790.1:p.Ser1132=
XM_006723728.2:c.3367T=	XP_006723791.1:p.Ser1123=
XM_006723730.2:c.3313T=	XP_006723793.1:p.Ser1105=
XM_006723732.2:c.3214T=	XP_006723795.1:p.Ser1072=
XM_006723733.1:c.2713T=	XP_006723796.1:p.Ser905=
XM_011528647.1:c.3661T=	XP_011526949.1:p.Ser1221=
XM_011528648.1:c.3658T=	XP_011526950.1:p.Ser1220=
XM_011528649.1:c.3577T=	XP_011526951.1:p.Ser1193=
XM_011528650.1:c.3508T=	XP_011526952.1:p.Ser1170=
XM_011528651.1:c.3376T=	XP_011526953.1:p.Ser1126=
XM_011528652.1:c.3313T=	XP_011526954.1:p.Ser1105=
NM_001363734.1:c.3214T=	NP_001350663.1:p.Ser1072=
XM_006723727.3:c.3394T=	XP_006723790.1:p.Ser1132=
XM_006723728.3:c.3367T=	XP_006723791.1:p.Ser1123=
XM_006723730.4:c.3313T=	XP_006723793.1:p.Ser1105=
XM_011528648.3:c.3658T=	XP_011526950.1:p.Ser1220=
XM_011528652.2:c.3313T=	XP_011526954.1:p.Ser1105=
XM_017027704.1:c.3313T=	XP_016883193.1:p.Ser1105=
XM_017027705.1:c.3313T=	XP_016883194.1:p.Ser1105=
XM_017027706.1:c.3244T=	XP_016883195.1:p.Ser1082=
NM_015338.6:c.3397T= MANE Select	NP_056153.2:p.Ser1133=