Canonical Allele Identifier: CA2391112032
Gene: U2AF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43094609G= , CM000683.2:g.43094609G= GRCh38
NG_029455.1:g.17970C= , LRG_615:g.17970C=

Transcript Alleles

HGVS Amino-acid change
ENST00000291552.9:c.483-46C= MANE Select ENSP00000291552.4:n.483-46C=
ENST00000291552.8:c.483-46C= ENSP00000291552.4:n.483-46C=
ENST00000380276.6:c.483-46C= ENSP00000369629.2:n.483-46C=
ENST00000398137.5:c.264-46C= ENSP00000381205.1:n.264-46C=
ENST00000459639.5:c.264-46C= ENSP00000418705.1:n.264-46C=
ENST00000464750.5:c.*322-46C= ENSP00000420672.1:n.*322-46C=
ENST00000471250.5:n.1290-46C=
ENST00000475639.5:n.4308-46C=
ENST00000478282.1:n.1737-46C=
ENST00000486519.5:n.530-46C=
NM_001025203.1:c.483-46C= , LRG_615t1:c.483-46C= NP_001020374.1:n.483-46C=
NM_001025204.1:c.264-46C= NP_001020375.1:n.264-46C=
NM_006758.2:c.483-46C= , LRG_615t2:c.483-46C= NP_006749.1:n.483-46C=
XM_011529743.1:c.384-46C= XP_011528045.1:n.384-46C=
XM_011529743.3:c.384-46C= XP_011528045.1:n.384-46C=
XM_017028468.2:c.384-46C= XP_016883957.1:n.384-46C=
XM_024452129.1:c.264-46C= XP_024307897.1:n.264-46C=
XM_024452130.1:c.264-46C= XP_024307898.1:n.264-46C=
XM_024452131.1:c.264-46C= XP_024307899.1:n.264-46C=
NM_001025204.2:c.264-46C= NP_001020375.1:n.264-46C=
NM_006758.3:c.483-46C= MANE Select NP_006749.1:n.483-46C=