Canonical Allele Identifier: CA2360293510

Gene: ASXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436048G= , CM000682.2:g.32436048G=	GRCh38
NC_000020.10:g.31023851G= , CM000682.1:g.31023851G=	GRCh37
NC_000020.9:g.30487512G=	NCBI36
NG_027868.1:g.82705G= , LRG_630:g.82705G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3336G= MANE Select	ENSP00000364839.4:p.Leu1112=
ENST00000646985.1:c.3153G=	ENSP00000495053.1:p.Leu1051=
ENST00000647223.1:n.5689G=
ENST00000651418.1:c.1869+1467G=	ENSP00000499150.1:n.1869+1467G=
ENST00000306058.9:c.3321G=	ENSP00000305119.5:p.Leu1107=
ENST00000375687.8:c.3336G=	ENSP00000364839.4:p.Leu1112=
ENST00000613218.4:c.3336G=	ENSP00000480487.1:p.Leu1112=
ENST00000620121.4:c.3336G=	ENSP00000481978.1:p.Leu1112=
NM_015338.5:c.3336G= , LRG_630t1:c.3336G=	NP_056153.2:p.Leu1112=
XM_006723727.2:c.3333G=	XP_006723790.1:p.Leu1111=
XM_006723728.2:c.3306G=	XP_006723791.1:p.Leu1102=
XM_006723730.2:c.3252G=	XP_006723793.1:p.Leu1084=
XM_006723732.2:c.3153G=	XP_006723795.1:p.Leu1051=
XM_006723733.1:c.2652G=	XP_006723796.1:p.Leu884=
XM_011528647.1:c.3600G=	XP_011526949.1:p.Leu1200=
XM_011528648.1:c.3597G=	XP_011526950.1:p.Leu1199=
XM_011528649.1:c.3516G=	XP_011526951.1:p.Leu1172=
XM_011528650.1:c.3447G=	XP_011526952.1:p.Leu1149=
XM_011528651.1:c.3315G=	XP_011526953.1:p.Leu1105=
XM_011528652.1:c.3252G=	XP_011526954.1:p.Leu1084=
NM_001363734.1:c.3153G=	NP_001350663.1:p.Leu1051=
XM_006723727.3:c.3333G=	XP_006723790.1:p.Leu1111=
XM_006723728.3:c.3306G=	XP_006723791.1:p.Leu1102=
XM_006723730.4:c.3252G=	XP_006723793.1:p.Leu1084=
XM_011528648.3:c.3597G=	XP_011526950.1:p.Leu1199=
XM_011528652.2:c.3252G=	XP_011526954.1:p.Leu1084=
XM_017027704.1:c.3252G=	XP_016883193.1:p.Leu1084=
XM_017027705.1:c.3252G=	XP_016883194.1:p.Leu1084=
XM_017027706.1:c.3183G=	XP_016883195.1:p.Leu1061=
NM_015338.6:c.3336G= MANE Select	NP_056153.2:p.Leu1112=