Canonical Allele Identifier: CA2360293821

Gene: ASXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436693T= , CM000682.2:g.32436693T=	GRCh38
NC_000020.10:g.31024496T= , CM000682.1:g.31024496T=	GRCh37
NC_000020.9:g.30488157T=	NCBI36
NG_027868.1:g.83350T= , LRG_630:g.83350T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3981T= MANE Select	ENSP00000364839.4:p.Ala1327=
ENST00000646985.1:c.3798T=	ENSP00000495053.1:p.Ala1266=
ENST00000647223.1:n.6334T=
ENST00000651418.1:c.1870-1737T=	ENSP00000499150.1:n.1870-1737T=
ENST00000306058.9:c.3966T=	ENSP00000305119.5:p.Ala1322=
ENST00000375687.8:c.3981T=	ENSP00000364839.4:p.Ala1327=
ENST00000613218.4:c.3981T=	ENSP00000480487.1:p.Ala1327=
ENST00000620121.4:c.3981T=	ENSP00000481978.1:p.Ala1327=
NM_015338.5:c.3981T= , LRG_630t1:c.3981T=	NP_056153.2:p.Ala1327=
XM_006723727.2:c.3978T=	XP_006723790.1:p.Ala1326=
XM_006723728.2:c.3951T=	XP_006723791.1:p.Ala1317=
XM_006723730.2:c.3897T=	XP_006723793.1:p.Ala1299=
XM_006723732.2:c.3798T=	XP_006723795.1:p.Ala1266=
XM_006723733.1:c.3297T=	XP_006723796.1:p.Ala1099=
XM_011528647.1:c.4245T=	XP_011526949.1:p.Ala1415=
XM_011528648.1:c.4242T=	XP_011526950.1:p.Ala1414=
XM_011528649.1:c.4161T=	XP_011526951.1:p.Ala1387=
XM_011528650.1:c.4092T=	XP_011526952.1:p.Ala1364=
XM_011528651.1:c.3960T=	XP_011526953.1:p.Ala1320=
XM_011528652.1:c.3897T=	XP_011526954.1:p.Ala1299=
NM_001363734.1:c.3798T=	NP_001350663.1:p.Ala1266=
XM_006723727.3:c.3978T=	XP_006723790.1:p.Ala1326=
XM_006723728.3:c.3951T=	XP_006723791.1:p.Ala1317=
XM_006723730.4:c.3897T=	XP_006723793.1:p.Ala1299=
XM_011528648.3:c.4242T=	XP_011526950.1:p.Ala1414=
XM_011528652.2:c.3897T=	XP_011526954.1:p.Ala1299=
XM_017027704.1:c.3897T=	XP_016883193.1:p.Ala1299=
XM_017027705.1:c.3897T=	XP_016883194.1:p.Ala1299=
XM_017027706.1:c.3828T=	XP_016883195.1:p.Ala1276=
NM_015338.6:c.3981T= MANE Select	NP_056153.2:p.Ala1327=