Canonical Allele Identifier: CA2360293518

Gene: ASXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436071A= , CM000682.2:g.32436071A=	GRCh38
NC_000020.10:g.31023874A= , CM000682.1:g.31023874A=	GRCh37
NC_000020.9:g.30487535A=	NCBI36
NG_027868.1:g.82728A= , LRG_630:g.82728A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3359A= MANE Select	ENSP00000364839.4:p.Lys1120=
ENST00000646985.1:c.3176A=	ENSP00000495053.1:p.Lys1059=
ENST00000647223.1:n.5712A=
ENST00000651418.1:c.1869+1490A=	ENSP00000499150.1:n.1869+1490A=
ENST00000306058.9:c.3344A=	ENSP00000305119.5:p.Lys1115=
ENST00000375687.8:c.3359A=	ENSP00000364839.4:p.Lys1120=
ENST00000613218.4:c.3359A=	ENSP00000480487.1:p.Lys1120=
ENST00000620121.4:c.3359A=	ENSP00000481978.1:p.Lys1120=
NM_015338.5:c.3359A= , LRG_630t1:c.3359A=	NP_056153.2:p.Lys1120=
XM_006723727.2:c.3356A=	XP_006723790.1:p.Lys1119=
XM_006723728.2:c.3329A=	XP_006723791.1:p.Lys1110=
XM_006723730.2:c.3275A=	XP_006723793.1:p.Lys1092=
XM_006723732.2:c.3176A=	XP_006723795.1:p.Lys1059=
XM_006723733.1:c.2675A=	XP_006723796.1:p.Lys892=
XM_011528647.1:c.3623A=	XP_011526949.1:p.Lys1208=
XM_011528648.1:c.3620A=	XP_011526950.1:p.Lys1207=
XM_011528649.1:c.3539A=	XP_011526951.1:p.Lys1180=
XM_011528650.1:c.3470A=	XP_011526952.1:p.Lys1157=
XM_011528651.1:c.3338A=	XP_011526953.1:p.Lys1113=
XM_011528652.1:c.3275A=	XP_011526954.1:p.Lys1092=
NM_001363734.1:c.3176A=	NP_001350663.1:p.Lys1059=
XM_006723727.3:c.3356A=	XP_006723790.1:p.Lys1119=
XM_006723728.3:c.3329A=	XP_006723791.1:p.Lys1110=
XM_006723730.4:c.3275A=	XP_006723793.1:p.Lys1092=
XM_011528648.3:c.3620A=	XP_011526950.1:p.Lys1207=
XM_011528652.2:c.3275A=	XP_011526954.1:p.Lys1092=
XM_017027704.1:c.3275A=	XP_016883193.1:p.Lys1092=
XM_017027705.1:c.3275A=	XP_016883194.1:p.Lys1092=
XM_017027706.1:c.3206A=	XP_016883195.1:p.Lys1069=
NM_015338.6:c.3359A= MANE Select	NP_056153.2:p.Lys1120=