Canonical Allele Identifier: CA408551386

Gene: ASXL1

Linked Data

• COSMIC: COSM6402299 ; COSM6402300
• MyVariant Identifiers: chr20:g.31015962C>T (hg19) ; chr20:g.32428159C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32428159C>T , CM000682.2:g.32428159C>T	GRCh38
NC_000020.10:g.31015962C>T , CM000682.1:g.31015962C>T	GRCh37
NC_000020.9:g.30479623C>T	NCBI36
NG_027868.1:g.74816C>T , LRG_630:g.74816C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.284C>T MANE Select	ENSP00000364839.4:p.Ala95Val
ENST00000470145.3:n.227C>T
ENST00000643168.1:c.200C>T	ENSP00000495003.1:p.Ala67Val
ENST00000644060.1:n.1088C>T
ENST00000644587.1:c.*123C>T	ENSP00000494813.1:n.*123C>T
ENST00000645514.1:n.32C>T
ENST00000645688.1:c.200C>T	ENSP00000495488.1:p.Ala67Val
ENST00000646985.1:c.254C>T	ENSP00000495053.1:p.Ala85Val
ENST00000651418.1:c.284C>T	ENSP00000499150.1:p.Ala95Val
ENST00000306058.9:c.269C>T	ENSP00000305119.5:p.Ala90Val
ENST00000375687.8:c.284C>T	ENSP00000364839.4:p.Ala95Val
ENST00000470145.2:n.227C>T
ENST00000613218.4:c.284C>T	ENSP00000480487.1:p.Ala95Val
ENST00000620121.4:c.284C>T	ENSP00000481978.1:p.Ala95Val
NM_015338.5:c.284C>T , LRG_630t1:c.284C>T	NP_056153.2:p.Ala95Val
XM_006723727.2:c.281C>T	XP_006723790.1:p.Ala94Val
XM_006723728.2:c.254C>T	XP_006723791.1:p.Ala85Val
XM_006723730.2:c.200C>T	XP_006723793.1:p.Ala67Val
XM_006723732.2:c.254C>T	XP_006723795.1:p.Ala85Val
XM_011528647.1:c.548C>T	XP_011526949.1:p.Ala183Val
XM_011528648.1:c.545C>T	XP_011526950.1:p.Ala182Val
XM_011528649.1:c.464C>T	XP_011526951.1:p.Ala155Val
XM_011528650.1:c.548C>T	XP_011526952.1:p.Ala183Val
XM_011528651.1:c.263C>T	XP_011526953.1:p.Ala88Val
XM_011528652.1:c.200C>T	XP_011526954.1:p.Ala67Val
NM_001363734.1:c.254C>T	NP_001350663.1:p.Ala85Val
XM_006723727.3:c.281C>T	XP_006723790.1:p.Ala94Val
XM_006723728.3:c.254C>T	XP_006723791.1:p.Ala85Val
XM_006723730.4:c.200C>T	XP_006723793.1:p.Ala67Val
XM_011528648.3:c.545C>T	XP_011526950.1:p.Ala182Val
XM_011528652.2:c.200C>T	XP_011526954.1:p.Ala67Val
XM_017027704.1:c.200C>T	XP_016883193.1:p.Ala67Val
XM_017027705.1:c.200C>T	XP_016883194.1:p.Ala67Val
XM_017027706.1:c.284C>T	XP_016883195.1:p.Ala95Val
NM_015338.6:c.284C>T MANE Select	NP_056153.2:p.Ala95Val