Canonical Allele Identifier: CA2360293464

Gene: ASXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32435930G= , CM000682.2:g.32435930G=	GRCh38
NC_000020.10:g.31023733G= , CM000682.1:g.31023733G=	GRCh37
NC_000020.9:g.30487394G=	NCBI36
NG_027868.1:g.82587G= , LRG_630:g.82587G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3218G= MANE Select	ENSP00000364839.4:p.Arg1073=
ENST00000646985.1:c.3035G=	ENSP00000495053.1:p.Arg1012=
ENST00000647223.1:n.5571G=
ENST00000651418.1:c.1869+1349G=	ENSP00000499150.1:n.1869+1349G=
ENST00000306058.9:c.3203G=	ENSP00000305119.5:p.Arg1068=
ENST00000375687.8:c.3218G=	ENSP00000364839.4:p.Arg1073=
ENST00000613218.4:c.3218G=	ENSP00000480487.1:p.Arg1073=
ENST00000620121.4:c.3218G=	ENSP00000481978.1:p.Arg1073=
NM_015338.5:c.3218G= , LRG_630t1:c.3218G=	NP_056153.2:p.Arg1073=
XM_006723727.2:c.3215G=	XP_006723790.1:p.Arg1072=
XM_006723728.2:c.3188G=	XP_006723791.1:p.Arg1063=
XM_006723730.2:c.3134G=	XP_006723793.1:p.Arg1045=
XM_006723732.2:c.3035G=	XP_006723795.1:p.Arg1012=
XM_006723733.1:c.2534G=	XP_006723796.1:p.Arg845=
XM_011528647.1:c.3482G=	XP_011526949.1:p.Arg1161=
XM_011528648.1:c.3479G=	XP_011526950.1:p.Arg1160=
XM_011528649.1:c.3398G=	XP_011526951.1:p.Arg1133=
XM_011528650.1:c.3329G=	XP_011526952.1:p.Arg1110=
XM_011528651.1:c.3197G=	XP_011526953.1:p.Arg1066=
XM_011528652.1:c.3134G=	XP_011526954.1:p.Arg1045=
NM_001363734.1:c.3035G=	NP_001350663.1:p.Arg1012=
XM_006723727.3:c.3215G=	XP_006723790.1:p.Arg1072=
XM_006723728.3:c.3188G=	XP_006723791.1:p.Arg1063=
XM_006723730.4:c.3134G=	XP_006723793.1:p.Arg1045=
XM_011528648.3:c.3479G=	XP_011526950.1:p.Arg1160=
XM_011528652.2:c.3134G=	XP_011526954.1:p.Arg1045=
XM_017027704.1:c.3134G=	XP_016883193.1:p.Arg1045=
XM_017027705.1:c.3134G=	XP_016883194.1:p.Arg1045=
XM_017027706.1:c.3065G=	XP_016883195.1:p.Arg1022=
NM_015338.6:c.3218G= MANE Select	NP_056153.2:p.Arg1073=