Canonical Allele Identifier: CA408564104

Gene: ASXL1

Linked Data

• dbSNP Id: rs148144203
• MyVariant Identifiers: chr20:g.31024450C>G (hg19) ; chr20:g.32436647C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436647C>G , CM000682.2:g.32436647C>G	GRCh38
NC_000020.10:g.31024450C>G , CM000682.1:g.31024450C>G	GRCh37
NC_000020.9:g.30488111C>G	NCBI36
NG_027868.1:g.83304C>G , LRG_630:g.83304C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3935C>G MANE Select	ENSP00000364839.4:p.Ala1312Gly
ENST00000646985.1:c.3752C>G	ENSP00000495053.1:p.Ala1251Gly
ENST00000647223.1:n.6288C>G
ENST00000651418.1:c.1870-1783C>G	ENSP00000499150.1:n.1870-1783C>G
ENST00000306058.9:c.3920C>G	ENSP00000305119.5:p.Ala1307Gly
ENST00000375687.8:c.3935C>G	ENSP00000364839.4:p.Ala1312Gly
ENST00000613218.4:c.3935C>G	ENSP00000480487.1:p.Ala1312Gly
ENST00000620121.4:c.3935C>G	ENSP00000481978.1:p.Ala1312Gly
NM_015338.5:c.3935C>G , LRG_630t1:c.3935C>G	NP_056153.2:p.Ala1312Gly
XM_006723727.2:c.3932C>G	XP_006723790.1:p.Ala1311Gly
XM_006723728.2:c.3905C>G	XP_006723791.1:p.Ala1302Gly
XM_006723730.2:c.3851C>G	XP_006723793.1:p.Ala1284Gly
XM_006723732.2:c.3752C>G	XP_006723795.1:p.Ala1251Gly
XM_006723733.1:c.3251C>G	XP_006723796.1:p.Ala1084Gly
XM_011528647.1:c.4199C>G	XP_011526949.1:p.Ala1400Gly
XM_011528648.1:c.4196C>G	XP_011526950.1:p.Ala1399Gly
XM_011528649.1:c.4115C>G	XP_011526951.1:p.Ala1372Gly
XM_011528650.1:c.4046C>G	XP_011526952.1:p.Ala1349Gly
XM_011528651.1:c.3914C>G	XP_011526953.1:p.Ala1305Gly
XM_011528652.1:c.3851C>G	XP_011526954.1:p.Ala1284Gly
NM_001363734.1:c.3752C>G	NP_001350663.1:p.Ala1251Gly
XM_006723727.3:c.3932C>G	XP_006723790.1:p.Ala1311Gly
XM_006723728.3:c.3905C>G	XP_006723791.1:p.Ala1302Gly
XM_006723730.4:c.3851C>G	XP_006723793.1:p.Ala1284Gly
XM_011528648.3:c.4196C>G	XP_011526950.1:p.Ala1399Gly
XM_011528652.2:c.3851C>G	XP_011526954.1:p.Ala1284Gly
XM_017027704.1:c.3851C>G	XP_016883193.1:p.Ala1284Gly
XM_017027705.1:c.3851C>G	XP_016883194.1:p.Ala1284Gly
XM_017027706.1:c.3782C>G	XP_016883195.1:p.Ala1261Gly
NM_015338.6:c.3935C>G MANE Select	NP_056153.2:p.Ala1312Gly