Canonical Allele Identifier: CA2360293878

Gene: ASXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436807C= , CM000682.2:g.32436807C=	GRCh38
NC_000020.10:g.31024610C= , CM000682.1:g.31024610C=	GRCh37
NC_000020.9:g.30488271C=	NCBI36
NG_027868.1:g.83464C= , LRG_630:g.83464C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.4095C= MANE Select	ENSP00000364839.4:p.Gly1365=
ENST00000646985.1:c.3912C=	ENSP00000495053.1:p.Gly1304=
ENST00000647223.1:n.6448C=
ENST00000651418.1:c.1870-1623C=	ENSP00000499150.1:n.1870-1623C=
ENST00000306058.9:c.4080C=	ENSP00000305119.5:p.Gly1360=
ENST00000375687.8:c.4095C=	ENSP00000364839.4:p.Gly1365=
ENST00000613218.4:c.4095C=	ENSP00000480487.1:p.Gly1365=
ENST00000620121.4:c.4095C=	ENSP00000481978.1:p.Gly1365=
NM_015338.5:c.4095C= , LRG_630t1:c.4095C=	NP_056153.2:p.Gly1365=
XM_006723727.2:c.4092C=	XP_006723790.1:p.Gly1364=
XM_006723728.2:c.4065C=	XP_006723791.1:p.Gly1355=
XM_006723730.2:c.4011C=	XP_006723793.1:p.Gly1337=
XM_006723732.2:c.3912C=	XP_006723795.1:p.Gly1304=
XM_006723733.1:c.3411C=	XP_006723796.1:p.Gly1137=
XM_011528647.1:c.4359C=	XP_011526949.1:p.Gly1453=
XM_011528648.1:c.4356C=	XP_011526950.1:p.Gly1452=
XM_011528649.1:c.4275C=	XP_011526951.1:p.Gly1425=
XM_011528650.1:c.4206C=	XP_011526952.1:p.Gly1402=
XM_011528651.1:c.4074C=	XP_011526953.1:p.Gly1358=
XM_011528652.1:c.4011C=	XP_011526954.1:p.Gly1337=
NM_001363734.1:c.3912C=	NP_001350663.1:p.Gly1304=
XM_006723727.3:c.4092C=	XP_006723790.1:p.Gly1364=
XM_006723728.3:c.4065C=	XP_006723791.1:p.Gly1355=
XM_006723730.4:c.4011C=	XP_006723793.1:p.Gly1337=
XM_011528648.3:c.4356C=	XP_011526950.1:p.Gly1452=
XM_011528652.2:c.4011C=	XP_011526954.1:p.Gly1337=
XM_017027704.1:c.4011C=	XP_016883193.1:p.Gly1337=
XM_017027705.1:c.4011C=	XP_016883194.1:p.Gly1337=
XM_017027706.1:c.3942C=	XP_016883195.1:p.Gly1314=
NM_015338.6:c.4095C= MANE Select	NP_056153.2:p.Gly1365=