Canonical Allele Identifier: CA2360293780

Gene: ASXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436591_32436592delinsTC , CM000682.2:g.32436591_32436592delinsTC	GRCh38
NC_000020.10:g.31024394_31024395delinsTC , CM000682.1:g.31024394_31024395delinsTC	GRCh37
NC_000020.9:g.30488055_30488056delinsTC	NCBI36
NG_027868.1:g.83248_83249delinsTC , LRG_630:g.83248_83249delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3879_3880delinsTC MANE Select	ENSP00000364839.4:p.Asp1293=
ENST00000646985.1:c.3696_3697delinsTC	ENSP00000495053.1:p.Asp1232=
ENST00000647223.1:n.6232_6233delinsTC
ENST00000651418.1:c.1870-1839_1870-1838delinsTC	ENSP00000499150.1:n.1870-1839_1870-1838delinsTC
ENST00000306058.9:c.3864_3865delinsTC	ENSP00000305119.5:p.Asp1288=
ENST00000375687.8:c.3879_3880delinsTC	ENSP00000364839.4:p.Asp1293=
ENST00000613218.4:c.3879_3880delinsTC	ENSP00000480487.1:p.Asp1293=
ENST00000620121.4:c.3879_3880delinsTC	ENSP00000481978.1:p.Asp1293=
NM_015338.5:c.3879_3880delinsTC , LRG_630t1:c.3879_3880delinsTC	NP_056153.2:p.Asp1293=
XM_006723727.2:c.3876_3877delinsTC	XP_006723790.1:p.Asp1292=
XM_006723728.2:c.3849_3850delinsTC	XP_006723791.1:p.Asp1283=
XM_006723730.2:c.3795_3796delinsTC	XP_006723793.1:p.Asp1265=
XM_006723732.2:c.3696_3697delinsTC	XP_006723795.1:p.Asp1232=
XM_006723733.1:c.3195_3196delinsTC	XP_006723796.1:p.Asp1065=
XM_011528647.1:c.4143_4144delinsTC	XP_011526949.1:p.Asp1381=
XM_011528648.1:c.4140_4141delinsTC	XP_011526950.1:p.Asp1380=
XM_011528649.1:c.4059_4060delinsTC	XP_011526951.1:p.Asp1353=
XM_011528650.1:c.3990_3991delinsTC	XP_011526952.1:p.Asp1330=
XM_011528651.1:c.3858_3859delinsTC	XP_011526953.1:p.Asp1286=
XM_011528652.1:c.3795_3796delinsTC	XP_011526954.1:p.Asp1265=
NM_001363734.1:c.3696_3697delinsTC	NP_001350663.1:p.Asp1232=
XM_006723727.3:c.3876_3877delinsTC	XP_006723790.1:p.Asp1292=
XM_006723728.3:c.3849_3850delinsTC	XP_006723791.1:p.Asp1283=
XM_006723730.4:c.3795_3796delinsTC	XP_006723793.1:p.Asp1265=
XM_011528648.3:c.4140_4141delinsTC	XP_011526950.1:p.Asp1380=
XM_011528652.2:c.3795_3796delinsTC	XP_011526954.1:p.Asp1265=
XM_017027704.1:c.3795_3796delinsTC	XP_016883193.1:p.Asp1265=
XM_017027705.1:c.3795_3796delinsTC	XP_016883194.1:p.Asp1265=
XM_017027706.1:c.3726_3727delinsTC	XP_016883195.1:p.Asp1242=
NM_015338.6:c.3879_3880delinsTC MANE Select	NP_056153.2:p.Asp1293=