Canonical Allele Identifier: CA408562846

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31023852C>G (hg19) ; chr20:g.32436049C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436049C>G , CM000682.2:g.32436049C>G	GRCh38
NC_000020.10:g.31023852C>G , CM000682.1:g.31023852C>G	GRCh37
NC_000020.9:g.30487513C>G	NCBI36
NG_027868.1:g.82706C>G , LRG_630:g.82706C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3337C>G MANE Select	ENSP00000364839.4:p.Gln1113Glu
ENST00000646985.1:c.3154C>G	ENSP00000495053.1:p.Gln1052Glu
ENST00000647223.1:n.5690C>G
ENST00000651418.1:c.1869+1468C>G	ENSP00000499150.1:n.1869+1468C>G
ENST00000306058.9:c.3322C>G	ENSP00000305119.5:p.Gln1108Glu
ENST00000375687.8:c.3337C>G	ENSP00000364839.4:p.Gln1113Glu
ENST00000613218.4:c.3337C>G	ENSP00000480487.1:p.Gln1113Glu
ENST00000620121.4:c.3337C>G	ENSP00000481978.1:p.Gln1113Glu
NM_015338.5:c.3337C>G , LRG_630t1:c.3337C>G	NP_056153.2:p.Gln1113Glu
XM_006723727.2:c.3334C>G	XP_006723790.1:p.Gln1112Glu
XM_006723728.2:c.3307C>G	XP_006723791.1:p.Gln1103Glu
XM_006723730.2:c.3253C>G	XP_006723793.1:p.Gln1085Glu
XM_006723732.2:c.3154C>G	XP_006723795.1:p.Gln1052Glu
XM_006723733.1:c.2653C>G	XP_006723796.1:p.Gln885Glu
XM_011528647.1:c.3601C>G	XP_011526949.1:p.Gln1201Glu
XM_011528648.1:c.3598C>G	XP_011526950.1:p.Gln1200Glu
XM_011528649.1:c.3517C>G	XP_011526951.1:p.Gln1173Glu
XM_011528650.1:c.3448C>G	XP_011526952.1:p.Gln1150Glu
XM_011528651.1:c.3316C>G	XP_011526953.1:p.Gln1106Glu
XM_011528652.1:c.3253C>G	XP_011526954.1:p.Gln1085Glu
NM_001363734.1:c.3154C>G	NP_001350663.1:p.Gln1052Glu
XM_006723727.3:c.3334C>G	XP_006723790.1:p.Gln1112Glu
XM_006723728.3:c.3307C>G	XP_006723791.1:p.Gln1103Glu
XM_006723730.4:c.3253C>G	XP_006723793.1:p.Gln1085Glu
XM_011528648.3:c.3598C>G	XP_011526950.1:p.Gln1200Glu
XM_011528652.2:c.3253C>G	XP_011526954.1:p.Gln1085Glu
XM_017027704.1:c.3253C>G	XP_016883193.1:p.Gln1085Glu
XM_017027705.1:c.3253C>G	XP_016883194.1:p.Gln1085Glu
XM_017027706.1:c.3184C>G	XP_016883195.1:p.Gln1062Glu
NM_015338.6:c.3337C>G MANE Select	NP_056153.2:p.Gln1113Glu