Canonical Allele Identifier: CA408552008

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31016193A>T (hg19) ; chr20:g.32428390A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32428390A>T , CM000682.2:g.32428390A>T	GRCh38
NC_000020.10:g.31016193A>T , CM000682.1:g.31016193A>T	GRCh37
NC_000020.9:g.30479854A>T	NCBI36
NG_027868.1:g.75047A>T , LRG_630:g.75047A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.439A>T MANE Select	ENSP00000364839.4:p.Asn147Tyr
ENST00000470145.3:n.458A>T
ENST00000643168.1:c.355A>T	ENSP00000495003.1:p.Asn119Tyr
ENST00000644587.1:c.*278A>T	ENSP00000494813.1:n.*278A>T
ENST00000644615.1:n.143A>T
ENST00000645514.1:n.263A>T
ENST00000646985.1:c.409A>T	ENSP00000495053.1:p.Asn137Tyr
ENST00000651418.1:c.439A>T	ENSP00000499150.1:p.Asn147Tyr
ENST00000306058.9:c.424A>T	ENSP00000305119.5:p.Asn142Tyr
ENST00000375687.8:c.439A>T	ENSP00000364839.4:p.Asn147Tyr
ENST00000470145.2:n.458A>T
ENST00000613218.4:c.439A>T	ENSP00000480487.1:p.Asn147Tyr
ENST00000620121.4:c.439A>T	ENSP00000481978.1:p.Asn147Tyr
NM_015338.5:c.439A>T , LRG_630t1:c.439A>T	NP_056153.2:p.Asn147Tyr
XM_006723727.2:c.436A>T	XP_006723790.1:p.Asn146Tyr
XM_006723728.2:c.409A>T	XP_006723791.1:p.Asn137Tyr
XM_006723730.2:c.355A>T	XP_006723793.1:p.Asn119Tyr
XM_006723732.2:c.409A>T	XP_006723795.1:p.Asn137Tyr
XM_011528647.1:c.703A>T	XP_011526949.1:p.Asn235Tyr
XM_011528648.1:c.700A>T	XP_011526950.1:p.Asn234Tyr
XM_011528649.1:c.619A>T	XP_011526951.1:p.Asn207Tyr
XM_011528650.1:c.703A>T	XP_011526952.1:p.Asn235Tyr
XM_011528651.1:c.418A>T	XP_011526953.1:p.Asn140Tyr
XM_011528652.1:c.355A>T	XP_011526954.1:p.Asn119Tyr
NM_001363734.1:c.409A>T	NP_001350663.1:p.Asn137Tyr
XM_006723727.3:c.436A>T	XP_006723790.1:p.Asn146Tyr
XM_006723728.3:c.409A>T	XP_006723791.1:p.Asn137Tyr
XM_006723730.4:c.355A>T	XP_006723793.1:p.Asn119Tyr
XM_011528648.3:c.700A>T	XP_011526950.1:p.Asn234Tyr
XM_011528652.2:c.355A>T	XP_011526954.1:p.Asn119Tyr
XM_017027704.1:c.355A>T	XP_016883193.1:p.Asn119Tyr
XM_017027705.1:c.355A>T	XP_016883194.1:p.Asn119Tyr
XM_017027706.1:c.439A>T	XP_016883195.1:p.Asn147Tyr
NM_015338.6:c.439A>T MANE Select	NP_056153.2:p.Asn147Tyr