Canonical Allele Identifier: CA408551828

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31016152A>G (hg19) ; chr20:g.32428349A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32428349A>G , CM000682.2:g.32428349A>G	GRCh38
NC_000020.10:g.31016152A>G , CM000682.1:g.31016152A>G	GRCh37
NC_000020.9:g.30479813A>G	NCBI36
NG_027868.1:g.75006A>G , LRG_630:g.75006A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.398A>G MANE Select	ENSP00000364839.4:p.Asn133Ser
ENST00000470145.3:n.417A>G
ENST00000643168.1:c.314A>G	ENSP00000495003.1:p.Asn105Ser
ENST00000644060.1:n.1202A>G
ENST00000644587.1:c.*237A>G	ENSP00000494813.1:n.*237A>G
ENST00000644615.1:n.102A>G
ENST00000645514.1:n.222A>G
ENST00000646985.1:c.368A>G	ENSP00000495053.1:p.Asn123Ser
ENST00000651418.1:c.398A>G	ENSP00000499150.1:p.Asn133Ser
ENST00000306058.9:c.383A>G	ENSP00000305119.5:p.Asn128Ser
ENST00000375687.8:c.398A>G	ENSP00000364839.4:p.Asn133Ser
ENST00000470145.2:n.417A>G
ENST00000613218.4:c.398A>G	ENSP00000480487.1:p.Asn133Ser
ENST00000620121.4:c.398A>G	ENSP00000481978.1:p.Asn133Ser
NM_015338.5:c.398A>G , LRG_630t1:c.398A>G	NP_056153.2:p.Asn133Ser
XM_006723727.2:c.395A>G	XP_006723790.1:p.Asn132Ser
XM_006723728.2:c.368A>G	XP_006723791.1:p.Asn123Ser
XM_006723730.2:c.314A>G	XP_006723793.1:p.Asn105Ser
XM_006723732.2:c.368A>G	XP_006723795.1:p.Asn123Ser
XM_011528647.1:c.662A>G	XP_011526949.1:p.Asn221Ser
XM_011528648.1:c.659A>G	XP_011526950.1:p.Asn220Ser
XM_011528649.1:c.578A>G	XP_011526951.1:p.Asn193Ser
XM_011528650.1:c.662A>G	XP_011526952.1:p.Asn221Ser
XM_011528651.1:c.377A>G	XP_011526953.1:p.Asn126Ser
XM_011528652.1:c.314A>G	XP_011526954.1:p.Asn105Ser
NM_001363734.1:c.368A>G	NP_001350663.1:p.Asn123Ser
XM_006723727.3:c.395A>G	XP_006723790.1:p.Asn132Ser
XM_006723728.3:c.368A>G	XP_006723791.1:p.Asn123Ser
XM_006723730.4:c.314A>G	XP_006723793.1:p.Asn105Ser
XM_011528648.3:c.659A>G	XP_011526950.1:p.Asn220Ser
XM_011528652.2:c.314A>G	XP_011526954.1:p.Asn105Ser
XM_017027704.1:c.314A>G	XP_016883193.1:p.Asn105Ser
XM_017027705.1:c.314A>G	XP_016883194.1:p.Asn105Ser
XM_017027706.1:c.398A>G	XP_016883195.1:p.Asn133Ser
NM_015338.6:c.398A>G MANE Select	NP_056153.2:p.Asn133Ser