Canonical Allele Identifier: CA2360293815

Gene: ASXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436679A= , CM000682.2:g.32436679A=	GRCh38
NC_000020.10:g.31024482A= , CM000682.1:g.31024482A=	GRCh37
NC_000020.9:g.30488143A=	NCBI36
NG_027868.1:g.83336A= , LRG_630:g.83336A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3967A= MANE Select	ENSP00000364839.4:p.Met1323=
ENST00000646985.1:c.3784A=	ENSP00000495053.1:p.Met1262=
ENST00000647223.1:n.6320A=
ENST00000651418.1:c.1870-1751A=	ENSP00000499150.1:n.1870-1751A=
ENST00000306058.9:c.3952A=	ENSP00000305119.5:p.Met1318=
ENST00000375687.8:c.3967A=	ENSP00000364839.4:p.Met1323=
ENST00000613218.4:c.3967A=	ENSP00000480487.1:p.Met1323=
ENST00000620121.4:c.3967A=	ENSP00000481978.1:p.Met1323=
NM_015338.5:c.3967A= , LRG_630t1:c.3967A=	NP_056153.2:p.Met1323=
XM_006723727.2:c.3964A=	XP_006723790.1:p.Met1322=
XM_006723728.2:c.3937A=	XP_006723791.1:p.Met1313=
XM_006723730.2:c.3883A=	XP_006723793.1:p.Met1295=
XM_006723732.2:c.3784A=	XP_006723795.1:p.Met1262=
XM_006723733.1:c.3283A=	XP_006723796.1:p.Met1095=
XM_011528647.1:c.4231A=	XP_011526949.1:p.Met1411=
XM_011528648.1:c.4228A=	XP_011526950.1:p.Met1410=
XM_011528649.1:c.4147A=	XP_011526951.1:p.Met1383=
XM_011528650.1:c.4078A=	XP_011526952.1:p.Met1360=
XM_011528651.1:c.3946A=	XP_011526953.1:p.Met1316=
XM_011528652.1:c.3883A=	XP_011526954.1:p.Met1295=
NM_001363734.1:c.3784A=	NP_001350663.1:p.Met1262=
XM_006723727.3:c.3964A=	XP_006723790.1:p.Met1322=
XM_006723728.3:c.3937A=	XP_006723791.1:p.Met1313=
XM_006723730.4:c.3883A=	XP_006723793.1:p.Met1295=
XM_011528648.3:c.4228A=	XP_011526950.1:p.Met1410=
XM_011528652.2:c.3883A=	XP_011526954.1:p.Met1295=
XM_017027704.1:c.3883A=	XP_016883193.1:p.Met1295=
XM_017027705.1:c.3883A=	XP_016883194.1:p.Met1295=
XM_017027706.1:c.3814A=	XP_016883195.1:p.Met1272=
NM_015338.6:c.3967A= MANE Select	NP_056153.2:p.Met1323=