Canonical Allele Identifier: CA510467628

Gene: ASXL1

Linked Data

• gnomAD v4: 20-32436762-G-A
• MyVariant Identifiers: chr20:g.31024565G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436762G>A , CM000682.2:g.32436762G>A	GRCh38
NC_000020.10:g.31024565G>A , CM000682.1:g.31024565G>A	GRCh37
NC_000020.9:g.30488226G>A	NCBI36
NG_027868.1:g.83419G>A , LRG_630:g.83419G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.4050G>A MANE Select	ENSP00000364839.4:p.Gln1350=
ENST00000646985.1:c.3867G>A	ENSP00000495053.1:p.Gln1289=
ENST00000647223.1:n.6403G>A
ENST00000651418.1:c.1870-1668G>A	ENSP00000499150.1:n.1870-1668G>A
ENST00000306058.9:c.4035G>A	ENSP00000305119.5:p.Gln1345=
ENST00000375687.8:c.4050G>A	ENSP00000364839.4:p.Gln1350=
ENST00000613218.4:c.4050G>A	ENSP00000480487.1:p.Gln1350=
ENST00000620121.4:c.4050G>A	ENSP00000481978.1:p.Gln1350=
NM_015338.5:c.4050G>A , LRG_630t1:c.4050G>A	NP_056153.2:p.Gln1350=
XM_006723727.2:c.4047G>A	XP_006723790.1:p.Gln1349=
XM_006723728.2:c.4020G>A	XP_006723791.1:p.Gln1340=
XM_006723730.2:c.3966G>A	XP_006723793.1:p.Gln1322=
XM_006723732.2:c.3867G>A	XP_006723795.1:p.Gln1289=
XM_006723733.1:c.3366G>A	XP_006723796.1:p.Gln1122=
XM_011528647.1:c.4314G>A	XP_011526949.1:p.Gln1438=
XM_011528648.1:c.4311G>A	XP_011526950.1:p.Gln1437=
XM_011528649.1:c.4230G>A	XP_011526951.1:p.Gln1410=
XM_011528650.1:c.4161G>A	XP_011526952.1:p.Gln1387=
XM_011528651.1:c.4029G>A	XP_011526953.1:p.Gln1343=
XM_011528652.1:c.3966G>A	XP_011526954.1:p.Gln1322=
NM_001363734.1:c.3867G>A	NP_001350663.1:p.Gln1289=
XM_006723727.3:c.4047G>A	XP_006723790.1:p.Gln1349=
XM_006723728.3:c.4020G>A	XP_006723791.1:p.Gln1340=
XM_006723730.4:c.3966G>A	XP_006723793.1:p.Gln1322=
XM_011528648.3:c.4311G>A	XP_011526950.1:p.Gln1437=
XM_011528652.2:c.3966G>A	XP_011526954.1:p.Gln1322=
XM_017027704.1:c.3966G>A	XP_016883193.1:p.Gln1322=
XM_017027705.1:c.3966G>A	XP_016883194.1:p.Gln1322=
XM_017027706.1:c.3897G>A	XP_016883195.1:p.Gln1299=
NM_015338.6:c.4050G>A MANE Select	NP_056153.2:p.Gln1350=