Canonical Allele Identifier: CA2360293499

Gene: ASXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436027C= , CM000682.2:g.32436027C=	GRCh38
NC_000020.10:g.31023830C= , CM000682.1:g.31023830C=	GRCh37
NC_000020.9:g.30487491C=	NCBI36
NG_027868.1:g.82684C= , LRG_630:g.82684C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3315C= MANE Select	ENSP00000364839.4:p.Asn1105=
ENST00000646985.1:c.3132C=	ENSP00000495053.1:p.Asn1044=
ENST00000647223.1:n.5668C=
ENST00000651418.1:c.1869+1446C=	ENSP00000499150.1:n.1869+1446C=
ENST00000306058.9:c.3300C=	ENSP00000305119.5:p.Asn1100=
ENST00000375687.8:c.3315C=	ENSP00000364839.4:p.Asn1105=
ENST00000613218.4:c.3315C=	ENSP00000480487.1:p.Asn1105=
ENST00000620121.4:c.3315C=	ENSP00000481978.1:p.Asn1105=
NM_015338.5:c.3315C= , LRG_630t1:c.3315C=	NP_056153.2:p.Asn1105=
XM_006723727.2:c.3312C=	XP_006723790.1:p.Asn1104=
XM_006723728.2:c.3285C=	XP_006723791.1:p.Asn1095=
XM_006723730.2:c.3231C=	XP_006723793.1:p.Asn1077=
XM_006723732.2:c.3132C=	XP_006723795.1:p.Asn1044=
XM_006723733.1:c.2631C=	XP_006723796.1:p.Asn877=
XM_011528647.1:c.3579C=	XP_011526949.1:p.Asn1193=
XM_011528648.1:c.3576C=	XP_011526950.1:p.Asn1192=
XM_011528649.1:c.3495C=	XP_011526951.1:p.Asn1165=
XM_011528650.1:c.3426C=	XP_011526952.1:p.Asn1142=
XM_011528651.1:c.3294C=	XP_011526953.1:p.Asn1098=
XM_011528652.1:c.3231C=	XP_011526954.1:p.Asn1077=
NM_001363734.1:c.3132C=	NP_001350663.1:p.Asn1044=
XM_006723727.3:c.3312C=	XP_006723790.1:p.Asn1104=
XM_006723728.3:c.3285C=	XP_006723791.1:p.Asn1095=
XM_006723730.4:c.3231C=	XP_006723793.1:p.Asn1077=
XM_011528648.3:c.3576C=	XP_011526950.1:p.Asn1192=
XM_011528652.2:c.3231C=	XP_011526954.1:p.Asn1077=
XM_017027704.1:c.3231C=	XP_016883193.1:p.Asn1077=
XM_017027705.1:c.3231C=	XP_016883194.1:p.Asn1077=
XM_017027706.1:c.3162C=	XP_016883195.1:p.Asn1054=
NM_015338.6:c.3315C= MANE Select	NP_056153.2:p.Asn1105=