Canonical Allele Identifier: CA413249729
Gene: PHF8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.54042654C>T , CM000685.2:g.54042654C>T GRCh38
NC_000023.10:g.54069087C>T , CM000685.1:g.54069087C>T GRCh37
NC_000023.9:g.54085812C>T NCBI36
NG_021309.1:g.7483G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338946.11:c.75G>A ENSP00000340051.7:p.Met25Ile
ENST00000396282.7:c.75G>A ENSP00000379578.3:p.Met25Ile
ENST00000686349.1:c.75G>A ENSP00000510424.1:p.Met25Ile
ENST00000687764.1:c.75G>A ENSP00000509967.1:p.Met25Ile
ENST00000338154.11:c.75G>A MANE Select ENSP00000338868.6:p.Met25Ile
ENST00000322659.12:c.75G>A ENSP00000319473.8:p.Met25Ile
ENST00000338154.10:c.75G>A ENSP00000338868.6:p.Met25Ile
ENST00000338946.10:c.75G>A ENSP00000340051.6:p.Met25Ile
ENST00000357988.9:c.183G>A ENSP00000350676.5:p.Met61Ile
ENST00000415025.5:c.75G>A ENSP00000404117.1:p.Met25Ile
ENST00000425862.5:c.75G>A ENSP00000408113.1:p.Met25Ile
ENST00000433120.5:c.75G>A ENSP00000410100.1:p.Met25Ile
ENST00000437224.5:c.75G>A ENSP00000398995.1:p.Met25Ile
ENST00000445025.1:c.75G>A ENSP00000416546.1:p.Met25Ile
ENST00000453905.5:c.183G>A ENSP00000405897.1:p.Met61Ile
ENST00000462182.1:n.63G>A
NM_001184896.1:c.183G>A NP_001171825.1:p.Met61Ile
NM_001184897.1:c.75G>A NP_001171826.1:p.Met25Ile
NM_001184898.1:c.75G>A NP_001171827.1:p.Met25Ile
NM_015107.2:c.75G>A NP_055922.1:p.Met25Ile
XM_005261996.1:c.183G>A XP_005262053.1:p.Met61Ile
XM_005261997.2:c.75G>A XP_005262054.1:p.Met25Ile
XM_005261999.1:c.75G>A XP_005262056.1:p.Met25Ile
XM_005262000.1:c.183G>A XP_005262057.1:p.Met61Ile
XM_006724585.1:c.183G>A XP_006724648.1:p.Met61Ile
XM_011530778.1:c.183G>A XP_011529080.1:p.Met61Ile
XM_005261997.4:c.75G>A XP_005262054.1:p.Met25Ile
XM_017029361.2:c.75G>A XP_016884850.1:p.Met25Ile
XM_017029362.2:c.75G>A XP_016884851.1:p.Met25Ile
NM_001184898.2:c.75G>A NP_001171827.1:p.Met25Ile
NM_015107.3:c.75G>A MANE Select NP_055922.1:p.Met25Ile
NM_001184897.2:c.75G>A NP_001171826.1:p.Met25Ile