Canonical Allele Identifier: CA2360293833

Gene: ASXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436724T= , CM000682.2:g.32436724T=	GRCh38
NC_000020.10:g.31024527T= , CM000682.1:g.31024527T=	GRCh37
NC_000020.9:g.30488188T=	NCBI36
NG_027868.1:g.83381T= , LRG_630:g.83381T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.4012T= MANE Select	ENSP00000364839.4:p.Leu1338=
ENST00000646985.1:c.3829T=	ENSP00000495053.1:p.Leu1277=
ENST00000647223.1:n.6365T=
ENST00000651418.1:c.1870-1706T=	ENSP00000499150.1:n.1870-1706T=
ENST00000306058.9:c.3997T=	ENSP00000305119.5:p.Leu1333=
ENST00000375687.8:c.4012T=	ENSP00000364839.4:p.Leu1338=
ENST00000613218.4:c.4012T=	ENSP00000480487.1:p.Leu1338=
ENST00000620121.4:c.4012T=	ENSP00000481978.1:p.Leu1338=
NM_015338.5:c.4012T= , LRG_630t1:c.4012T=	NP_056153.2:p.Leu1338=
XM_006723727.2:c.4009T=	XP_006723790.1:p.Leu1337=
XM_006723728.2:c.3982T=	XP_006723791.1:p.Leu1328=
XM_006723730.2:c.3928T=	XP_006723793.1:p.Leu1310=
XM_006723732.2:c.3829T=	XP_006723795.1:p.Leu1277=
XM_006723733.1:c.3328T=	XP_006723796.1:p.Leu1110=
XM_011528647.1:c.4276T=	XP_011526949.1:p.Leu1426=
XM_011528648.1:c.4273T=	XP_011526950.1:p.Leu1425=
XM_011528649.1:c.4192T=	XP_011526951.1:p.Leu1398=
XM_011528650.1:c.4123T=	XP_011526952.1:p.Leu1375=
XM_011528651.1:c.3991T=	XP_011526953.1:p.Leu1331=
XM_011528652.1:c.3928T=	XP_011526954.1:p.Leu1310=
NM_001363734.1:c.3829T=	NP_001350663.1:p.Leu1277=
XM_006723727.3:c.4009T=	XP_006723790.1:p.Leu1337=
XM_006723728.3:c.3982T=	XP_006723791.1:p.Leu1328=
XM_006723730.4:c.3928T=	XP_006723793.1:p.Leu1310=
XM_011528648.3:c.4273T=	XP_011526950.1:p.Leu1425=
XM_011528652.2:c.3928T=	XP_011526954.1:p.Leu1310=
XM_017027704.1:c.3928T=	XP_016883193.1:p.Leu1310=
XM_017027705.1:c.3928T=	XP_016883194.1:p.Leu1310=
XM_017027706.1:c.3859T=	XP_016883195.1:p.Leu1287=
NM_015338.6:c.4012T= MANE Select	NP_056153.2:p.Leu1338=