Canonical Allele Identifier: CA2360293562

Gene: ASXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436158T= , CM000682.2:g.32436158T=	GRCh38
NC_000020.10:g.31023961T= , CM000682.1:g.31023961T=	GRCh37
NC_000020.9:g.30487622T=	NCBI36
NG_027868.1:g.82815T= , LRG_630:g.82815T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3446T= MANE Select	ENSP00000364839.4:p.Met1149=
ENST00000646985.1:c.3263T=	ENSP00000495053.1:p.Met1088=
ENST00000647223.1:n.5799T=
ENST00000651418.1:c.1869+1577T=	ENSP00000499150.1:n.1869+1577T=
ENST00000306058.9:c.3431T=	ENSP00000305119.5:p.Met1144=
ENST00000375687.8:c.3446T=	ENSP00000364839.4:p.Met1149=
ENST00000613218.4:c.3446T=	ENSP00000480487.1:p.Met1149=
ENST00000620121.4:c.3446T=	ENSP00000481978.1:p.Met1149=
NM_015338.5:c.3446T= , LRG_630t1:c.3446T=	NP_056153.2:p.Met1149=
XM_006723727.2:c.3443T=	XP_006723790.1:p.Met1148=
XM_006723728.2:c.3416T=	XP_006723791.1:p.Met1139=
XM_006723730.2:c.3362T=	XP_006723793.1:p.Met1121=
XM_006723732.2:c.3263T=	XP_006723795.1:p.Met1088=
XM_006723733.1:c.2762T=	XP_006723796.1:p.Met921=
XM_011528647.1:c.3710T=	XP_011526949.1:p.Met1237=
XM_011528648.1:c.3707T=	XP_011526950.1:p.Met1236=
XM_011528649.1:c.3626T=	XP_011526951.1:p.Met1209=
XM_011528650.1:c.3557T=	XP_011526952.1:p.Met1186=
XM_011528651.1:c.3425T=	XP_011526953.1:p.Met1142=
XM_011528652.1:c.3362T=	XP_011526954.1:p.Met1121=
NM_001363734.1:c.3263T=	NP_001350663.1:p.Met1088=
XM_006723727.3:c.3443T=	XP_006723790.1:p.Met1148=
XM_006723728.3:c.3416T=	XP_006723791.1:p.Met1139=
XM_006723730.4:c.3362T=	XP_006723793.1:p.Met1121=
XM_011528648.3:c.3707T=	XP_011526950.1:p.Met1236=
XM_011528652.2:c.3362T=	XP_011526954.1:p.Met1121=
XM_017027704.1:c.3362T=	XP_016883193.1:p.Met1121=
XM_017027705.1:c.3362T=	XP_016883194.1:p.Met1121=
XM_017027706.1:c.3293T=	XP_016883195.1:p.Met1098=
NM_015338.6:c.3446T= MANE Select	NP_056153.2:p.Met1149=