Canonical Allele Identifier: CA388198347
Gene: PHF11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.49515708C>A , CM000675.2:g.49515708C>A GRCh38
NC_000013.10:g.50089844C>A , CM000675.1:g.50089844C>A GRCh37
NC_000013.9:g.48987845C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378319.8:c.325-2310C>A MANE Select ENSP00000367570.3:n.325-2310C>A
ENST00000357596.7:c.208-2310C>A ENSP00000350209.3:n.208-2310C>A
ENST00000378319.7:c.325-2310C>A ENSP00000367570.3:n.325-2310C>A
ENST00000426879.5:c.189-2310C>A
ENST00000442195.5:c.208-2310C>A ENSP00000405227.1:n.208-2310C>A
ENST00000465045.5:c.208-2310C>A ENSP00000418630.1:n.208-2310C>A
ENST00000467763.5:n.505-2310C>A
ENST00000476953.6:n.192-2310C>A
ENST00000481509.5:n.540-2310C>A
ENST00000482487.5:n.717-2310C>A
ENST00000485919.5:c.208-2310C>A ENSP00000420129.1:n.208-2310C>A
ENST00000487433.6:n.484-2310C>A
ENST00000488958.5:c.208-2310C>A ENSP00000417539.1:n.208-2310C>A
ENST00000496612.5:c.121-2310C>A ENSP00000419229.1:n.121-2310C>A
ENST00000496623.5:c.325-2310C>A ENSP00000483500.1:n.325-2310C>A
ENST00000621822.4:c.208-2310C>A ENSP00000482432.1:n.208-2310C>A
NM_001040443.1:c.325-2310C>A NP_001035533.1:n.325-2310C>A
NM_001040444.1:c.208-2310C>A NP_001035534.1:n.208-2310C>A
XM_006719828.2:c.325-2310C>A XP_006719891.1:n.325-2310C>A
XM_006719829.1:c.208-2310C>A XP_006719892.1:n.208-2310C>A
XM_006719830.1:c.208-2310C>A XP_006719893.1:n.208-2310C>A
XM_011535102.1:c.208-2310C>A XP_011533404.1:n.208-2310C>A
XR_245387.3:n.717-2310C>A
XR_941596.1:n.717-2310C>A
XR_941597.1:n.484-2310C>A
NM_001040443.2:c.325-2310C>A NP_001035533.1:n.325-2310C>A
NM_001040444.2:c.208-2310C>A NP_001035534.1:n.208-2310C>A
NM_001320727.1:c.1807-2310C>A NP_001307656.1:n.1807-2310C>A
NR_135322.1:n.595-2310C>A
NR_135323.1:n.529-2310C>A
NR_135324.1:n.2752-2310C>A
NM_001040443.3:c.325-2310C>A MANE Select NP_001035533.1:n.325-2310C>A
NM_001320727.2:c.1807-2310C>A NP_001307656.1:n.1807-2310C>A
NR_135322.2:n.252-2310C>A
NR_135323.2:n.479-2310C>A
NR_135324.2:n.2771-2310C>A