Canonical Allele Identifier: CA3028458070

Gene: U2AF1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.43104264T>G , CM000683.2:g.43104264T>G	GRCh38
NG_029455.1:g.8315A>C , LRG_615:g.8315A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006758.3:c.132+51A>C MANE Select	NP_006749.1:n.132+51A>C
ENST00000291552.9:c.132+51A>C MANE Select	ENSP00000291552.4:n.132+51A>C
NM_001025203.1:c.132+51A>C , LRG_615t1:c.132+51A>C	NP_001020374.1:n.132+51A>C
NM_001025204.1:c.-155+51A>C	NP_001020375.1:n.-155+51A>C
NM_001025204.2:c.-155+51A>C	NP_001020375.1:n.-155+51A>C
NM_006758.2:c.132+51A>C , LRG_615t2:c.132+51A>C	NP_006749.1:n.132+51A>C
ENST00000291552.8:c.132+51A>C	ENSP00000291552.4:n.132+51A>C
ENST00000380276.6:c.132+51A>C	ENSP00000369629.2:n.132+51A>C
ENST00000398137.5:c.-155+51A>C	ENSP00000381205.1:n.-155+51A>C
ENST00000459639.5:c.-88+51A>C	ENSP00000418705.1:n.-88+51A>C
ENST00000463599.5:n.162+51A>C
ENST00000464750.5:c.132+51A>C	ENSP00000420672.1:n.132+51A>C
ENST00000475639.5:n.213A>C
ENST00000486519.5:n.208+51A>C
ENST00000496462.1:n.162+51A>C
XM_011529743.1:c.132+51A>C	XP_011528045.1:n.132+51A>C
XM_011529743.3:c.132+51A>C	XP_011528045.1:n.132+51A>C
XM_017028468.2:c.132+51A>C	XP_016883957.1:n.132+51A>C
XM_024452129.1:c.-88+51A>C	XP_024307897.1:n.-88+51A>C
XM_024452130.1:c.-88+51A>C	XP_024307898.1:n.-88+51A>C
XM_024452131.1:c.-88+51A>C	XP_024307899.1:n.-88+51A>C