Canonical Allele Identifier: CA2573106233

Gene: U2AF1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.43094664_43094669dup , CM000683.2:g.43094664_43094669dup	GRCh38
NG_029455.1:g.17911_17916dup , LRG_615:g.17911_17916dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291552.9:c.469_474dup MANE Select	ENSP00000291552.4:p.Tyr158_Glu159insGlnTyr
ENST00000291552.8:c.469_474dup	ENSP00000291552.4:p.Tyr158_Glu159insGlnTyr
ENST00000380276.6:c.469_474dup	ENSP00000369629.2:p.Tyr158_Glu159insGlnTyr
ENST00000398137.5:c.250_255dup	ENSP00000381205.1:p.Tyr85_Glu86insGlnTyr
ENST00000459639.5:c.250_255dup	ENSP00000418705.1:p.Tyr85_Glu86insGlnTyr
ENST00000464750.5:c.*308_*313dup	ENSP00000420672.1:n.*308_*313dup
ENST00000471250.5:n.1276_1281dup
ENST00000475639.5:n.4294_4299dup
ENST00000478282.1:n.1723_1728dup
ENST00000486519.5:n.516_521dup
NM_001025203.1:c.469_474dup , LRG_615t1:c.469_474dup	NP_001020374.1:p.Tyr158_Glu159insGlnTyr
NM_001025204.1:c.250_255dup	NP_001020375.1:p.Tyr85_Glu86insGlnTyr
NM_006758.2:c.469_474dup , LRG_615t2:c.469_474dup	NP_006749.1:p.Tyr158_Glu159insGlnTyr
XM_011529743.1:c.370_375dup	XP_011528045.1:p.Tyr125_Glu126insGlnTyr
XM_011529743.3:c.370_375dup	XP_011528045.1:p.Tyr125_Glu126insGlnTyr
XM_017028468.2:c.370_375dup	XP_016883957.1:p.Tyr125_Glu126insGlnTyr
XM_024452129.1:c.250_255dup	XP_024307897.1:p.Tyr85_Glu86insGlnTyr
XM_024452130.1:c.250_255dup	XP_024307898.1:p.Tyr85_Glu86insGlnTyr
XM_024452131.1:c.250_255dup	XP_024307899.1:p.Tyr85_Glu86insGlnTyr
NM_001025204.2:c.250_255dup	NP_001020375.1:p.Tyr85_Glu86insGlnTyr
NM_006758.3:c.469_474dup MANE Select	NP_006749.1:p.Tyr158_Glu159insGlnTyr