Canonical Allele Identifier: CA2360293826

Gene: ASXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436701C= , CM000682.2:g.32436701C=	GRCh38
NC_000020.10:g.31024504C= , CM000682.1:g.31024504C=	GRCh37
NC_000020.9:g.30488165C=	NCBI36
NG_027868.1:g.83358C= , LRG_630:g.83358C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3989C= MANE Select	ENSP00000364839.4:p.Pro1330=
ENST00000646985.1:c.3806C=	ENSP00000495053.1:p.Pro1269=
ENST00000647223.1:n.6342C=
ENST00000651418.1:c.1870-1729C=	ENSP00000499150.1:n.1870-1729C=
ENST00000306058.9:c.3974C=	ENSP00000305119.5:p.Pro1325=
ENST00000375687.8:c.3989C=	ENSP00000364839.4:p.Pro1330=
ENST00000613218.4:c.3989C=	ENSP00000480487.1:p.Pro1330=
ENST00000620121.4:c.3989C=	ENSP00000481978.1:p.Pro1330=
NM_015338.5:c.3989C= , LRG_630t1:c.3989C=	NP_056153.2:p.Pro1330=
XM_006723727.2:c.3986C=	XP_006723790.1:p.Pro1329=
XM_006723728.2:c.3959C=	XP_006723791.1:p.Pro1320=
XM_006723730.2:c.3905C=	XP_006723793.1:p.Pro1302=
XM_006723732.2:c.3806C=	XP_006723795.1:p.Pro1269=
XM_006723733.1:c.3305C=	XP_006723796.1:p.Pro1102=
XM_011528647.1:c.4253C=	XP_011526949.1:p.Pro1418=
XM_011528648.1:c.4250C=	XP_011526950.1:p.Pro1417=
XM_011528649.1:c.4169C=	XP_011526951.1:p.Pro1390=
XM_011528650.1:c.4100C=	XP_011526952.1:p.Pro1367=
XM_011528651.1:c.3968C=	XP_011526953.1:p.Pro1323=
XM_011528652.1:c.3905C=	XP_011526954.1:p.Pro1302=
NM_001363734.1:c.3806C=	NP_001350663.1:p.Pro1269=
XM_006723727.3:c.3986C=	XP_006723790.1:p.Pro1329=
XM_006723728.3:c.3959C=	XP_006723791.1:p.Pro1320=
XM_006723730.4:c.3905C=	XP_006723793.1:p.Pro1302=
XM_011528648.3:c.4250C=	XP_011526950.1:p.Pro1417=
XM_011528652.2:c.3905C=	XP_011526954.1:p.Pro1302=
XM_017027704.1:c.3905C=	XP_016883193.1:p.Pro1302=
XM_017027705.1:c.3905C=	XP_016883194.1:p.Pro1302=
XM_017027706.1:c.3836C=	XP_016883195.1:p.Pro1279=
NM_015338.6:c.3989C= MANE Select	NP_056153.2:p.Pro1330=