Canonical Allele Identifier: CA510467168

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31023884A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436081A>T , CM000682.2:g.32436081A>T	GRCh38
NC_000020.10:g.31023884A>T , CM000682.1:g.31023884A>T	GRCh37
NC_000020.9:g.30487545A>T	NCBI36
NG_027868.1:g.82738A>T , LRG_630:g.82738A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3369A>T MANE Select	ENSP00000364839.4:p.Pro1123=
ENST00000646985.1:c.3186A>T	ENSP00000495053.1:p.Pro1062=
ENST00000647223.1:n.5722A>T
ENST00000651418.1:c.1869+1500A>T	ENSP00000499150.1:n.1869+1500A>T
ENST00000306058.9:c.3354A>T	ENSP00000305119.5:p.Pro1118=
ENST00000375687.8:c.3369A>T	ENSP00000364839.4:p.Pro1123=
ENST00000613218.4:c.3369A>T	ENSP00000480487.1:p.Pro1123=
ENST00000620121.4:c.3369A>T	ENSP00000481978.1:p.Pro1123=
NM_015338.5:c.3369A>T , LRG_630t1:c.3369A>T	NP_056153.2:p.Pro1123=
XM_006723727.2:c.3366A>T	XP_006723790.1:p.Pro1122=
XM_006723728.2:c.3339A>T	XP_006723791.1:p.Pro1113=
XM_006723730.2:c.3285A>T	XP_006723793.1:p.Pro1095=
XM_006723732.2:c.3186A>T	XP_006723795.1:p.Pro1062=
XM_006723733.1:c.2685A>T	XP_006723796.1:p.Pro895=
XM_011528647.1:c.3633A>T	XP_011526949.1:p.Pro1211=
XM_011528648.1:c.3630A>T	XP_011526950.1:p.Pro1210=
XM_011528649.1:c.3549A>T	XP_011526951.1:p.Pro1183=
XM_011528650.1:c.3480A>T	XP_011526952.1:p.Pro1160=
XM_011528651.1:c.3348A>T	XP_011526953.1:p.Pro1116=
XM_011528652.1:c.3285A>T	XP_011526954.1:p.Pro1095=
NM_001363734.1:c.3186A>T	NP_001350663.1:p.Pro1062=
XM_006723727.3:c.3366A>T	XP_006723790.1:p.Pro1122=
XM_006723728.3:c.3339A>T	XP_006723791.1:p.Pro1113=
XM_006723730.4:c.3285A>T	XP_006723793.1:p.Pro1095=
XM_011528648.3:c.3630A>T	XP_011526950.1:p.Pro1210=
XM_011528652.2:c.3285A>T	XP_011526954.1:p.Pro1095=
XM_017027704.1:c.3285A>T	XP_016883193.1:p.Pro1095=
XM_017027705.1:c.3285A>T	XP_016883194.1:p.Pro1095=
XM_017027706.1:c.3216A>T	XP_016883195.1:p.Pro1072=
NM_015338.6:c.3369A>T MANE Select	NP_056153.2:p.Pro1123=