Canonical Allele Identifier: CA2573334526
Gene: U2AF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43094666_43094667delinsTG , CM000683.2:g.43094666_43094667delinsTG GRCh38
NG_029455.1:g.17912_17913delinsCA , LRG_615:g.17912_17913delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000291552.9:c.470_471delinsCA MANE Select ENSP00000291552.4:p.Gln157Pro
ENST00000291552.8:c.470_471delinsCA ENSP00000291552.4:p.Gln157Pro
ENST00000380276.6:c.470_471delinsCA ENSP00000369629.2:p.Gln157Pro
ENST00000398137.5:c.251_252delinsCA ENSP00000381205.1:p.Gln84Pro
ENST00000459639.5:c.251_252delinsCA ENSP00000418705.1:p.Gln84Pro
ENST00000464750.5:c.*309_*310delinsCA ENSP00000420672.1:n.*309_*310delinsCA
ENST00000471250.5:n.1277_1278delinsCA
ENST00000475639.5:n.4295_4296delinsCA
ENST00000478282.1:n.1724_1725delinsCA
ENST00000486519.5:n.517_518delinsCA
NM_001025203.1:c.470_471delinsCA , LRG_615t1:c.470_471delinsCA NP_001020374.1:p.Gln157Pro
NM_001025204.1:c.251_252delinsCA NP_001020375.1:p.Gln84Pro
NM_006758.2:c.470_471delinsCA , LRG_615t2:c.470_471delinsCA NP_006749.1:p.Gln157Pro
XM_011529743.1:c.371_372delinsCA XP_011528045.1:p.Gln124Pro
XM_011529743.3:c.371_372delinsCA XP_011528045.1:p.Gln124Pro
XM_017028468.2:c.371_372delinsCA XP_016883957.1:p.Gln124Pro
XM_024452129.1:c.251_252delinsCA XP_024307897.1:p.Gln84Pro
XM_024452130.1:c.251_252delinsCA XP_024307898.1:p.Gln84Pro
XM_024452131.1:c.251_252delinsCA XP_024307899.1:p.Gln84Pro
NM_001025204.2:c.251_252delinsCA NP_001020375.1:p.Gln84Pro
NM_006758.3:c.470_471delinsCA MANE Select NP_006749.1:p.Gln157Pro