Canonical Allele Identifier: CA2360293847

Gene: ASXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436752G= , CM000682.2:g.32436752G=	GRCh38
NC_000020.10:g.31024555G= , CM000682.1:g.31024555G=	GRCh37
NC_000020.9:g.30488216G=	NCBI36
NG_027868.1:g.83409G= , LRG_630:g.83409G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.4040G= MANE Select	ENSP00000364839.4:p.Gly1347=
ENST00000646985.1:c.3857G=	ENSP00000495053.1:p.Gly1286=
ENST00000647223.1:n.6393G=
ENST00000651418.1:c.1870-1678G=	ENSP00000499150.1:n.1870-1678G=
ENST00000306058.9:c.4025G=	ENSP00000305119.5:p.Gly1342=
ENST00000375687.8:c.4040G=	ENSP00000364839.4:p.Gly1347=
ENST00000613218.4:c.4040G=	ENSP00000480487.1:p.Gly1347=
ENST00000620121.4:c.4040G=	ENSP00000481978.1:p.Gly1347=
NM_015338.5:c.4040G= , LRG_630t1:c.4040G=	NP_056153.2:p.Gly1347=
XM_006723727.2:c.4037G=	XP_006723790.1:p.Gly1346=
XM_006723728.2:c.4010G=	XP_006723791.1:p.Gly1337=
XM_006723730.2:c.3956G=	XP_006723793.1:p.Gly1319=
XM_006723732.2:c.3857G=	XP_006723795.1:p.Gly1286=
XM_006723733.1:c.3356G=	XP_006723796.1:p.Gly1119=
XM_011528647.1:c.4304G=	XP_011526949.1:p.Gly1435=
XM_011528648.1:c.4301G=	XP_011526950.1:p.Gly1434=
XM_011528649.1:c.4220G=	XP_011526951.1:p.Gly1407=
XM_011528650.1:c.4151G=	XP_011526952.1:p.Gly1384=
XM_011528651.1:c.4019G=	XP_011526953.1:p.Gly1340=
XM_011528652.1:c.3956G=	XP_011526954.1:p.Gly1319=
NM_001363734.1:c.3857G=	NP_001350663.1:p.Gly1286=
XM_006723727.3:c.4037G=	XP_006723790.1:p.Gly1346=
XM_006723728.3:c.4010G=	XP_006723791.1:p.Gly1337=
XM_006723730.4:c.3956G=	XP_006723793.1:p.Gly1319=
XM_011528648.3:c.4301G=	XP_011526950.1:p.Gly1434=
XM_011528652.2:c.3956G=	XP_011526954.1:p.Gly1319=
XM_017027704.1:c.3956G=	XP_016883193.1:p.Gly1319=
XM_017027705.1:c.3956G=	XP_016883194.1:p.Gly1319=
XM_017027706.1:c.3887G=	XP_016883195.1:p.Gly1296=
NM_015338.6:c.4040G= MANE Select	NP_056153.2:p.Gly1347=