Canonical Allele Identifier: CA510467029

Gene: ASXL1

Linked Data

• gnomAD v4: 20-32436030-A-G
• MyVariant Identifiers: chr20:g.31023833A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436030A>G , CM000682.2:g.32436030A>G	GRCh38
NC_000020.10:g.31023833A>G , CM000682.1:g.31023833A>G	GRCh37
NC_000020.9:g.30487494A>G	NCBI36
NG_027868.1:g.82687A>G , LRG_630:g.82687A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3318A>G MANE Select	ENSP00000364839.4:p.Pro1106=
ENST00000646985.1:c.3135A>G	ENSP00000495053.1:p.Pro1045=
ENST00000647223.1:n.5671A>G
ENST00000651418.1:c.1869+1449A>G	ENSP00000499150.1:n.1869+1449A>G
ENST00000306058.9:c.3303A>G	ENSP00000305119.5:p.Pro1101=
ENST00000375687.8:c.3318A>G	ENSP00000364839.4:p.Pro1106=
ENST00000613218.4:c.3318A>G	ENSP00000480487.1:p.Pro1106=
ENST00000620121.4:c.3318A>G	ENSP00000481978.1:p.Pro1106=
NM_015338.5:c.3318A>G , LRG_630t1:c.3318A>G	NP_056153.2:p.Pro1106=
XM_006723727.2:c.3315A>G	XP_006723790.1:p.Pro1105=
XM_006723728.2:c.3288A>G	XP_006723791.1:p.Pro1096=
XM_006723730.2:c.3234A>G	XP_006723793.1:p.Pro1078=
XM_006723732.2:c.3135A>G	XP_006723795.1:p.Pro1045=
XM_006723733.1:c.2634A>G	XP_006723796.1:p.Pro878=
XM_011528647.1:c.3582A>G	XP_011526949.1:p.Pro1194=
XM_011528648.1:c.3579A>G	XP_011526950.1:p.Pro1193=
XM_011528649.1:c.3498A>G	XP_011526951.1:p.Pro1166=
XM_011528650.1:c.3429A>G	XP_011526952.1:p.Pro1143=
XM_011528651.1:c.3297A>G	XP_011526953.1:p.Pro1099=
XM_011528652.1:c.3234A>G	XP_011526954.1:p.Pro1078=
NM_001363734.1:c.3135A>G	NP_001350663.1:p.Pro1045=
XM_006723727.3:c.3315A>G	XP_006723790.1:p.Pro1105=
XM_006723728.3:c.3288A>G	XP_006723791.1:p.Pro1096=
XM_006723730.4:c.3234A>G	XP_006723793.1:p.Pro1078=
XM_011528648.3:c.3579A>G	XP_011526950.1:p.Pro1193=
XM_011528652.2:c.3234A>G	XP_011526954.1:p.Pro1078=
XM_017027704.1:c.3234A>G	XP_016883193.1:p.Pro1078=
XM_017027705.1:c.3234A>G	XP_016883194.1:p.Pro1078=
XM_017027706.1:c.3165A>G	XP_016883195.1:p.Pro1055=
NM_015338.6:c.3318A>G MANE Select	NP_056153.2:p.Pro1106=