Canonical Allele Identifier: CA16602494
Community Standard Title: NM_006758.3(U2AF1):c.101C>T (p.Ser34Phe)
Gene: U2AF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43104346G>A , CM000683.2:g.43104346G>A GRCh38
NG_029455.1:g.8233C>T , LRG_615:g.8233C>T

Transcript Alleles

HGVS Amino-acid Change
NM_006758.3:c.101C>T MANE Select NP_006749.1:p.Ser34Phe
ENST00000291552.9:c.101C>T MANE Select ENSP00000291552.4:p.Ser34Phe
NM_001025203.1:c.101C>T , LRG_615t1:c.101C>T NP_001020374.1:p.Ser34Phe
NM_001025204.1:c.-186C>T NP_001020375.1:n.-186C>T
NM_001025204.2:c.-186C>T NP_001020375.1:n.-186C>T
NM_006758.2:c.101C>T , LRG_615t2:c.101C>T NP_006749.1:p.Ser34Phe
ENST00000291552.8:c.101C>T ENSP00000291552.4:p.Ser34Phe
ENST00000380276.6:c.101C>T ENSP00000369629.2:p.Ser34Phe
ENST00000398137.5:c.-186C>T ENSP00000381205.1:n.-186C>T
ENST00000459639.5:c.-119C>T ENSP00000418705.1:n.-119C>T
ENST00000463599.5:n.131C>T
ENST00000464750.5:c.101C>T ENSP00000420672.1:p.Ser34Phe
ENST00000475639.5:n.131C>T
ENST00000486519.5:n.177C>T
ENST00000496462.1:n.131C>T
XM_011529743.1:c.101C>T XP_011528045.1:p.Ser34Phe
XM_011529743.3:c.101C>T XP_011528045.1:p.Ser34Phe
XM_017028468.2:c.101C>T XP_016883957.1:p.Ser34Phe
XM_024452129.1:c.-119C>T XP_024307897.1:n.-119C>T
XM_024452130.1:c.-119C>T XP_024307898.1:n.-119C>T
XM_024452131.1:c.-119C>T XP_024307899.1:n.-119C>T