Canonical Allele Identifier: CA2391111998

Gene: U2AF1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.43094498C= , CM000683.2:g.43094498C=	GRCh38
NG_029455.1:g.18081G= , LRG_615:g.18081G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000291552.9:c.548G= MANE Select	ENSP00000291552.4:p.Arg183=
ENST00000291552.8:c.548G=	ENSP00000291552.4:p.Arg183=
ENST00000380276.6:c.548G=	ENSP00000369629.2:p.Arg183=
ENST00000398137.5:c.329G=	ENSP00000381205.1:p.Arg110=
ENST00000459639.5:c.329G=	ENSP00000418705.1:p.Arg110=
ENST00000464750.5:c.*387G=	ENSP00000420672.1:n.*387G=
ENST00000471250.5:n.1355G=
ENST00000475639.5:n.4373G=
ENST00000478282.1:n.1802G=
ENST00000486519.5:n.595G=
NM_001025203.1:c.548G= , LRG_615t1:c.548G=	NP_001020374.1:p.Arg183=
NM_001025204.1:c.329G=	NP_001020375.1:p.Arg110=
NM_006758.2:c.548G= , LRG_615t2:c.548G=	NP_006749.1:p.Arg183=
XM_011529743.1:c.449G=	XP_011528045.1:p.Arg150=
XM_011529743.3:c.449G=	XP_011528045.1:p.Arg150=
XM_017028468.2:c.449G=	XP_016883957.1:p.Arg150=
XM_024452129.1:c.329G=	XP_024307897.1:p.Arg110=
XM_024452130.1:c.329G=	XP_024307898.1:p.Arg110=
XM_024452131.1:c.329G=	XP_024307899.1:p.Arg110=
NM_001025204.2:c.329G=	NP_001020375.1:p.Arg110=
NM_006758.3:c.548G= MANE Select	NP_006749.1:p.Arg183=