Canonical Allele Identifier: CA408551583

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31016013G>T (hg19) ; chr20:g.32428210G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32428210G>T , CM000682.2:g.32428210G>T	GRCh38
NC_000020.10:g.31016013G>T , CM000682.1:g.31016013G>T	GRCh37
NC_000020.9:g.30479674G>T	NCBI36
NG_027868.1:g.74867G>T , LRG_630:g.74867G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.335G>T MANE Select	ENSP00000364839.4:p.Gly112Val
ENST00000470145.3:n.278G>T
ENST00000643168.1:c.251G>T	ENSP00000495003.1:p.Gly84Val
ENST00000644060.1:n.1139G>T
ENST00000644587.1:c.*174G>T	ENSP00000494813.1:n.*174G>T
ENST00000644615.1:n.39G>T
ENST00000645514.1:n.83G>T
ENST00000646985.1:c.305G>T	ENSP00000495053.1:p.Gly102Val
ENST00000651418.1:c.335G>T	ENSP00000499150.1:p.Gly112Val
ENST00000306058.9:c.320G>T	ENSP00000305119.5:p.Gly107Val
ENST00000375687.8:c.335G>T	ENSP00000364839.4:p.Gly112Val
ENST00000470145.2:n.278G>T
ENST00000613218.4:c.335G>T	ENSP00000480487.1:p.Gly112Val
ENST00000620121.4:c.335G>T	ENSP00000481978.1:p.Gly112Val
NM_015338.5:c.335G>T , LRG_630t1:c.335G>T	NP_056153.2:p.Gly112Val
XM_006723727.2:c.332G>T	XP_006723790.1:p.Gly111Val
XM_006723728.2:c.305G>T	XP_006723791.1:p.Gly102Val
XM_006723730.2:c.251G>T	XP_006723793.1:p.Gly84Val
XM_006723732.2:c.305G>T	XP_006723795.1:p.Gly102Val
XM_011528647.1:c.599G>T	XP_011526949.1:p.Gly200Val
XM_011528648.1:c.596G>T	XP_011526950.1:p.Gly199Val
XM_011528649.1:c.515G>T	XP_011526951.1:p.Gly172Val
XM_011528650.1:c.599G>T	XP_011526952.1:p.Gly200Val
XM_011528651.1:c.314G>T	XP_011526953.1:p.Gly105Val
XM_011528652.1:c.251G>T	XP_011526954.1:p.Gly84Val
NM_001363734.1:c.305G>T	NP_001350663.1:p.Gly102Val
XM_006723727.3:c.332G>T	XP_006723790.1:p.Gly111Val
XM_006723728.3:c.305G>T	XP_006723791.1:p.Gly102Val
XM_006723730.4:c.251G>T	XP_006723793.1:p.Gly84Val
XM_011528648.3:c.596G>T	XP_011526950.1:p.Gly199Val
XM_011528652.2:c.251G>T	XP_011526954.1:p.Gly84Val
XM_017027704.1:c.251G>T	XP_016883193.1:p.Gly84Val
XM_017027705.1:c.251G>T	XP_016883194.1:p.Gly84Val
XM_017027706.1:c.335G>T	XP_016883195.1:p.Gly112Val
NM_015338.6:c.335G>T MANE Select	NP_056153.2:p.Gly112Val