Canonical Allele Identifier: CA408561196

Gene: ASXL1

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32435485C>G , CM000682.2:g.32435485C>G	GRCh38
NC_000020.10:g.31023288C>G , CM000682.1:g.31023288C>G	GRCh37
NC_000020.9:g.30486949C>G	NCBI36
NG_027868.1:g.82142C>G , LRG_630:g.82142C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.2773C>G MANE Select	ENSP00000364839.4:p.Gln925Glu
ENST00000646985.1:c.2590C>G	ENSP00000495053.1:p.Gln864Glu
ENST00000647223.1:n.5126C>G
ENST00000651418.1:c.1869+904C>G	ENSP00000499150.1:n.1869+904C>G
ENST00000306058.9:c.2758C>G	ENSP00000305119.5:p.Gln920Glu
ENST00000375687.8:c.2773C>G	ENSP00000364839.4:p.Gln925Glu
ENST00000613218.4:c.2773C>G	ENSP00000480487.1:p.Gln925Glu
ENST00000620121.4:c.2773C>G	ENSP00000481978.1:p.Gln925Glu
NM_015338.5:c.2773C>G , LRG_630t1:c.2773C>G	NP_056153.2:p.Gln925Glu
XM_006723727.2:c.2770C>G	XP_006723790.1:p.Gln924Glu
XM_006723728.2:c.2743C>G	XP_006723791.1:p.Gln915Glu
XM_006723730.2:c.2689C>G	XP_006723793.1:p.Gln897Glu
XM_006723732.2:c.2590C>G	XP_006723795.1:p.Gln864Glu
XM_006723733.1:c.2089C>G	XP_006723796.1:p.Gln697Glu
XM_011528647.1:c.3037C>G	XP_011526949.1:p.Gln1013Glu
XM_011528648.1:c.3034C>G	XP_011526950.1:p.Gln1012Glu
XM_011528649.1:c.2953C>G	XP_011526951.1:p.Gln985Glu
XM_011528650.1:c.2884C>G	XP_011526952.1:p.Gln962Glu
XM_011528651.1:c.2752C>G	XP_011526953.1:p.Gln918Glu
XM_011528652.1:c.2689C>G	XP_011526954.1:p.Gln897Glu
NM_001363734.1:c.2590C>G	NP_001350663.1:p.Gln864Glu
XM_006723727.3:c.2770C>G	XP_006723790.1:p.Gln924Glu
XM_006723728.3:c.2743C>G	XP_006723791.1:p.Gln915Glu
XM_006723730.4:c.2689C>G	XP_006723793.1:p.Gln897Glu
XM_011528648.3:c.3034C>G	XP_011526950.1:p.Gln1012Glu
XM_011528652.2:c.2689C>G	XP_011526954.1:p.Gln897Glu
XM_017027704.1:c.2689C>G	XP_016883193.1:p.Gln897Glu
XM_017027705.1:c.2689C>G	XP_016883194.1:p.Gln897Glu
XM_017027706.1:c.2620C>G	XP_016883195.1:p.Gln874Glu
NM_015338.6:c.2773C>G MANE Select	NP_056153.2:p.Gln925Glu