Canonical Allele Identifier: CA510467534

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31024487T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436684T>A , CM000682.2:g.32436684T>A	GRCh38
NC_000020.10:g.31024487T>A , CM000682.1:g.31024487T>A	GRCh37
NC_000020.9:g.30488148T>A	NCBI36
NG_027868.1:g.83341T>A , LRG_630:g.83341T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3972T>A MANE Select	ENSP00000364839.4:p.Pro1324=
ENST00000646985.1:c.3789T>A	ENSP00000495053.1:p.Pro1263=
ENST00000647223.1:n.6325T>A
ENST00000651418.1:c.1870-1746T>A	ENSP00000499150.1:n.1870-1746T>A
ENST00000306058.9:c.3957T>A	ENSP00000305119.5:p.Pro1319=
ENST00000375687.8:c.3972T>A	ENSP00000364839.4:p.Pro1324=
ENST00000613218.4:c.3972T>A	ENSP00000480487.1:p.Pro1324=
ENST00000620121.4:c.3972T>A	ENSP00000481978.1:p.Pro1324=
NM_015338.5:c.3972T>A , LRG_630t1:c.3972T>A	NP_056153.2:p.Pro1324=
XM_006723727.2:c.3969T>A	XP_006723790.1:p.Pro1323=
XM_006723728.2:c.3942T>A	XP_006723791.1:p.Pro1314=
XM_006723730.2:c.3888T>A	XP_006723793.1:p.Pro1296=
XM_006723732.2:c.3789T>A	XP_006723795.1:p.Pro1263=
XM_006723733.1:c.3288T>A	XP_006723796.1:p.Pro1096=
XM_011528647.1:c.4236T>A	XP_011526949.1:p.Pro1412=
XM_011528648.1:c.4233T>A	XP_011526950.1:p.Pro1411=
XM_011528649.1:c.4152T>A	XP_011526951.1:p.Pro1384=
XM_011528650.1:c.4083T>A	XP_011526952.1:p.Pro1361=
XM_011528651.1:c.3951T>A	XP_011526953.1:p.Pro1317=
XM_011528652.1:c.3888T>A	XP_011526954.1:p.Pro1296=
NM_001363734.1:c.3789T>A	NP_001350663.1:p.Pro1263=
XM_006723727.3:c.3969T>A	XP_006723790.1:p.Pro1323=
XM_006723728.3:c.3942T>A	XP_006723791.1:p.Pro1314=
XM_006723730.4:c.3888T>A	XP_006723793.1:p.Pro1296=
XM_011528648.3:c.4233T>A	XP_011526950.1:p.Pro1411=
XM_011528652.2:c.3888T>A	XP_011526954.1:p.Pro1296=
XM_017027704.1:c.3888T>A	XP_016883193.1:p.Pro1296=
XM_017027705.1:c.3888T>A	XP_016883194.1:p.Pro1296=
XM_017027706.1:c.3819T>A	XP_016883195.1:p.Pro1273=
NM_015338.6:c.3972T>A MANE Select	NP_056153.2:p.Pro1324=