Canonical Allele Identifier: CA408564401

Gene: ASXL1

Linked Data

• ClinVar Variation Id: 1969637
• ClinVar RCV Id: RCV002717282
• dbSNP Id: rs1276856584
• gnomAD v2: 20-31024597-A-G
• gnomAD v3: 20-32436794-A-G
• gnomAD v4: 20-32436794-A-G
• MyVariant Identifiers: chr20:g.31024597A>G (hg19) ; chr20:g.32436794A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436794A>G , CM000682.2:g.32436794A>G	GRCh38
NC_000020.10:g.31024597A>G , CM000682.1:g.31024597A>G	GRCh37
NC_000020.9:g.30488258A>G	NCBI36
NG_027868.1:g.83451A>G , LRG_630:g.83451A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.4082A>G MANE Select	ENSP00000364839.4:p.His1361Arg
ENST00000646985.1:c.3899A>G	ENSP00000495053.1:p.His1300Arg
ENST00000647223.1:n.6435A>G
ENST00000651418.1:c.1870-1636A>G	ENSP00000499150.1:n.1870-1636A>G
ENST00000306058.9:c.4067A>G	ENSP00000305119.5:p.His1356Arg
ENST00000375687.8:c.4082A>G	ENSP00000364839.4:p.His1361Arg
ENST00000613218.4:c.4082A>G	ENSP00000480487.1:p.His1361Arg
ENST00000620121.4:c.4082A>G	ENSP00000481978.1:p.His1361Arg
NM_015338.5:c.4082A>G , LRG_630t1:c.4082A>G	NP_056153.2:p.His1361Arg
XM_006723727.2:c.4079A>G	XP_006723790.1:p.His1360Arg
XM_006723728.2:c.4052A>G	XP_006723791.1:p.His1351Arg
XM_006723730.2:c.3998A>G	XP_006723793.1:p.His1333Arg
XM_006723732.2:c.3899A>G	XP_006723795.1:p.His1300Arg
XM_006723733.1:c.3398A>G	XP_006723796.1:p.His1133Arg
XM_011528647.1:c.4346A>G	XP_011526949.1:p.His1449Arg
XM_011528648.1:c.4343A>G	XP_011526950.1:p.His1448Arg
XM_011528649.1:c.4262A>G	XP_011526951.1:p.His1421Arg
XM_011528650.1:c.4193A>G	XP_011526952.1:p.His1398Arg
XM_011528651.1:c.4061A>G	XP_011526953.1:p.His1354Arg
XM_011528652.1:c.3998A>G	XP_011526954.1:p.His1333Arg
NM_001363734.1:c.3899A>G	NP_001350663.1:p.His1300Arg
XM_006723727.3:c.4079A>G	XP_006723790.1:p.His1360Arg
XM_006723728.3:c.4052A>G	XP_006723791.1:p.His1351Arg
XM_006723730.4:c.3998A>G	XP_006723793.1:p.His1333Arg
XM_011528648.3:c.4343A>G	XP_011526950.1:p.His1448Arg
XM_011528652.2:c.3998A>G	XP_011526954.1:p.His1333Arg
XM_017027704.1:c.3998A>G	XP_016883193.1:p.His1333Arg
XM_017027705.1:c.3998A>G	XP_016883194.1:p.His1333Arg
XM_017027706.1:c.3929A>G	XP_016883195.1:p.His1310Arg
NM_015338.6:c.4082A>G MANE Select	NP_056153.2:p.His1361Arg