Canonical Allele Identifier: CA2360293666

Gene: ASXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436367C= , CM000682.2:g.32436367C=	GRCh38
NC_000020.10:g.31024170C= , CM000682.1:g.31024170C=	GRCh37
NC_000020.9:g.30487831C=	NCBI36
NG_027868.1:g.83024C= , LRG_630:g.83024C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3655C= MANE Select	ENSP00000364839.4:p.Pro1219=
ENST00000646985.1:c.3472C=	ENSP00000495053.1:p.Pro1158=
ENST00000647223.1:n.6008C=
ENST00000651418.1:c.1869+1786C=	ENSP00000499150.1:n.1869+1786C=
ENST00000306058.9:c.3640C=	ENSP00000305119.5:p.Pro1214=
ENST00000375687.8:c.3655C=	ENSP00000364839.4:p.Pro1219=
ENST00000613218.4:c.3655C=	ENSP00000480487.1:p.Pro1219=
ENST00000620121.4:c.3655C=	ENSP00000481978.1:p.Pro1219=
NM_015338.5:c.3655C= , LRG_630t1:c.3655C=	NP_056153.2:p.Pro1219=
XM_006723727.2:c.3652C=	XP_006723790.1:p.Pro1218=
XM_006723728.2:c.3625C=	XP_006723791.1:p.Pro1209=
XM_006723730.2:c.3571C=	XP_006723793.1:p.Pro1191=
XM_006723732.2:c.3472C=	XP_006723795.1:p.Pro1158=
XM_006723733.1:c.2971C=	XP_006723796.1:p.Pro991=
XM_011528647.1:c.3919C=	XP_011526949.1:p.Pro1307=
XM_011528648.1:c.3916C=	XP_011526950.1:p.Pro1306=
XM_011528649.1:c.3835C=	XP_011526951.1:p.Pro1279=
XM_011528650.1:c.3766C=	XP_011526952.1:p.Pro1256=
XM_011528651.1:c.3634C=	XP_011526953.1:p.Pro1212=
XM_011528652.1:c.3571C=	XP_011526954.1:p.Pro1191=
NM_001363734.1:c.3472C=	NP_001350663.1:p.Pro1158=
XM_006723727.3:c.3652C=	XP_006723790.1:p.Pro1218=
XM_006723728.3:c.3625C=	XP_006723791.1:p.Pro1209=
XM_006723730.4:c.3571C=	XP_006723793.1:p.Pro1191=
XM_011528648.3:c.3916C=	XP_011526950.1:p.Pro1306=
XM_011528652.2:c.3571C=	XP_011526954.1:p.Pro1191=
XM_017027704.1:c.3571C=	XP_016883193.1:p.Pro1191=
XM_017027705.1:c.3571C=	XP_016883194.1:p.Pro1191=
XM_017027706.1:c.3502C=	XP_016883195.1:p.Pro1168=
NM_015338.6:c.3655C= MANE Select	NP_056153.2:p.Pro1219=