Canonical Allele Identifier: CA2391112055

Gene: U2AF1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.43094670C= , CM000683.2:g.43094670C=	GRCh38
NG_029455.1:g.17909G= , LRG_615:g.17909G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291552.9:c.467G= MANE Select	ENSP00000291552.4:p.Arg156=
ENST00000291552.8:c.467G=	ENSP00000291552.4:p.Arg156=
ENST00000380276.6:c.467G=	ENSP00000369629.2:p.Arg156=
ENST00000398137.5:c.248G=	ENSP00000381205.1:p.Arg83=
ENST00000459639.5:c.248G=	ENSP00000418705.1:p.Arg83=
ENST00000464750.5:c.*306G=	ENSP00000420672.1:n.*306G=
ENST00000471250.5:n.1274G=
ENST00000475639.5:n.4292G=
ENST00000478282.1:n.1721G=
ENST00000486519.5:n.514G=
NM_001025203.1:c.467G= , LRG_615t1:c.467G=	NP_001020374.1:p.Arg156=
NM_001025204.1:c.248G=	NP_001020375.1:p.Arg83=
NM_006758.2:c.467G= , LRG_615t2:c.467G=	NP_006749.1:p.Arg156=
XM_011529743.1:c.368G=	XP_011528045.1:p.Arg123=
XM_011529743.3:c.368G=	XP_011528045.1:p.Arg123=
XM_017028468.2:c.368G=	XP_016883957.1:p.Arg123=
XM_024452129.1:c.248G=	XP_024307897.1:p.Arg83=
XM_024452130.1:c.248G=	XP_024307898.1:p.Arg83=
XM_024452131.1:c.248G=	XP_024307899.1:p.Arg83=
NM_001025204.2:c.248G=	NP_001020375.1:p.Arg83=
NM_006758.3:c.467G= MANE Select	NP_006749.1:p.Arg156=