Canonical Allele Identifier: CA408551380

Gene: ASXL1

Linked Data

• dbSNP Id: rs2011386443
• gnomAD v4: 20-32428158-G-A
• MyVariant Identifiers: chr20:g.31015961G>A (hg19) ; chr20:g.32428158G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32428158G>A , CM000682.2:g.32428158G>A	GRCh38
NC_000020.10:g.31015961G>A , CM000682.1:g.31015961G>A	GRCh37
NC_000020.9:g.30479622G>A	NCBI36
NG_027868.1:g.74815G>A , LRG_630:g.74815G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.283G>A MANE Select	ENSP00000364839.4:p.Ala95Thr
ENST00000470145.3:n.226G>A
ENST00000643168.1:c.199G>A	ENSP00000495003.1:p.Ala67Thr
ENST00000644060.1:n.1087G>A
ENST00000644587.1:c.*122G>A	ENSP00000494813.1:n.*122G>A
ENST00000645514.1:n.31G>A
ENST00000645688.1:c.199G>A	ENSP00000495488.1:p.Ala67Thr
ENST00000646985.1:c.253G>A	ENSP00000495053.1:p.Ala85Thr
ENST00000651418.1:c.283G>A	ENSP00000499150.1:p.Ala95Thr
ENST00000306058.9:c.268G>A	ENSP00000305119.5:p.Ala90Thr
ENST00000375687.8:c.283G>A	ENSP00000364839.4:p.Ala95Thr
ENST00000470145.2:n.226G>A
ENST00000613218.4:c.283G>A	ENSP00000480487.1:p.Ala95Thr
ENST00000620121.4:c.283G>A	ENSP00000481978.1:p.Ala95Thr
NM_015338.5:c.283G>A , LRG_630t1:c.283G>A	NP_056153.2:p.Ala95Thr
XM_006723727.2:c.280G>A	XP_006723790.1:p.Ala94Thr
XM_006723728.2:c.253G>A	XP_006723791.1:p.Ala85Thr
XM_006723730.2:c.199G>A	XP_006723793.1:p.Ala67Thr
XM_006723732.2:c.253G>A	XP_006723795.1:p.Ala85Thr
XM_011528647.1:c.547G>A	XP_011526949.1:p.Ala183Thr
XM_011528648.1:c.544G>A	XP_011526950.1:p.Ala182Thr
XM_011528649.1:c.463G>A	XP_011526951.1:p.Ala155Thr
XM_011528650.1:c.547G>A	XP_011526952.1:p.Ala183Thr
XM_011528651.1:c.262G>A	XP_011526953.1:p.Ala88Thr
XM_011528652.1:c.199G>A	XP_011526954.1:p.Ala67Thr
NM_001363734.1:c.253G>A	NP_001350663.1:p.Ala85Thr
XM_006723727.3:c.280G>A	XP_006723790.1:p.Ala94Thr
XM_006723728.3:c.253G>A	XP_006723791.1:p.Ala85Thr
XM_006723730.4:c.199G>A	XP_006723793.1:p.Ala67Thr
XM_011528648.3:c.544G>A	XP_011526950.1:p.Ala182Thr
XM_011528652.2:c.199G>A	XP_011526954.1:p.Ala67Thr
XM_017027704.1:c.199G>A	XP_016883193.1:p.Ala67Thr
XM_017027705.1:c.199G>A	XP_016883194.1:p.Ala67Thr
XM_017027706.1:c.283G>A	XP_016883195.1:p.Ala95Thr
NM_015338.6:c.283G>A MANE Select	NP_056153.2:p.Ala95Thr