Canonical Allele Identifier: CA157050

Gene: ASXL1

Linked Data

• PubMed: PMID:24728327

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32435156C= , CM000682.2:g.32435156C=	GRCh38
NG_027868.1:g.81813C= , LRG_630:g.81813C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.2444C= MANE Select	ENSP00000364839.4:p.Pro815=
ENST00000646985.1:c.2261C=	ENSP00000495053.1:p.Pro754=
ENST00000647223.1:n.4797C=
ENST00000651418.1:c.1869+575C=	ENSP00000499150.1:n.1869+575C=
ENST00000306058.9:c.2429C=	ENSP00000305119.5:p.Pro810=
ENST00000375687.8:c.2444C=	ENSP00000364839.4:p.Pro815=
ENST00000613218.4:c.2444C=	ENSP00000480487.1:p.Pro815=
ENST00000620121.4:c.2444C=	ENSP00000481978.1:p.Pro815=
NM_015338.5:c.2444C= , LRG_630t1:c.2444C=	NP_056153.2:p.Pro815=
XM_006723727.2:c.2441C=	XP_006723790.1:p.Pro814=
XM_006723728.2:c.2414C=	XP_006723791.1:p.Pro805=
XM_006723730.2:c.2360C=	XP_006723793.1:p.Pro787=
XM_006723732.2:c.2261C=	XP_006723795.1:p.Pro754=
XM_006723733.1:c.1760C=	XP_006723796.1:p.Pro587=
XM_011528647.1:c.2708C=	XP_011526949.1:p.Pro903=
XM_011528648.1:c.2705C=	XP_011526950.1:p.Pro902=
XM_011528649.1:c.2624C=	XP_011526951.1:p.Pro875=
XM_011528650.1:c.2555C=	XP_011526952.1:p.Pro852=
XM_011528651.1:c.2423C=	XP_011526953.1:p.Pro808=
XM_011528652.1:c.2360C=	XP_011526954.1:p.Pro787=
NM_001363734.1:c.2261C=	NP_001350663.1:p.Pro754=
XM_006723727.3:c.2441C=	XP_006723790.1:p.Pro814=
XM_006723728.3:c.2414C=	XP_006723791.1:p.Pro805=
XM_006723730.4:c.2360C=	XP_006723793.1:p.Pro787=
XM_011528648.3:c.2705C=	XP_011526950.1:p.Pro902=
XM_011528652.2:c.2360C=	XP_011526954.1:p.Pro787=
XM_017027704.1:c.2360C=	XP_016883193.1:p.Pro787=
XM_017027705.1:c.2360C=	XP_016883194.1:p.Pro787=
XM_017027706.1:c.2291C=	XP_016883195.1:p.Pro764=
NM_015338.6:c.2444C= MANE Select	NP_056153.2:p.Pro815=