Canonical Allele Identifier: CA2693828304
Gene: PHF8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53985341_53985345dup , CM000685.2:g.53985341_53985345dup GRCh38
NC_000023.10:g.54011774_54011778dup , CM000685.1:g.54011774_54011778dup GRCh37
NC_000023.9:g.54028499_54028503dup NCBI36
NG_021309.1:g.64792_64796dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000338946.11:c.1827-118_1827-114dup ENSP00000340051.7:n.1827-118_1827-114dup
ENST00000396282.7:c.2130-118_2130-114dup ENSP00000379578.3:n.2130-118_2130-114dup
ENST00000686349.1:c.*467_*471dup ENSP00000510424.1:n.*467_*471dup
ENST00000687764.1:c.*1454_*1458dup ENSP00000509967.1:n.*1454_*1458dup
ENST00000691629.1:n.1494-118_1494-114dup
ENST00000338154.11:c.2130-118_2130-114dup MANE Select ENSP00000338868.6:n.2130-118_2130-114dup
ENST00000322659.12:c.2079-118_2079-114dup ENSP00000319473.8:n.2079-118_2079-114dup
ENST00000338154.10:c.2130-118_2130-114dup ENSP00000338868.6:n.2130-118_2130-114dup
ENST00000338946.10:c.1827-118_1827-114dup ENSP00000340051.6:n.1827-118_1827-114dup
ENST00000357988.9:c.2238-118_2238-114dup ENSP00000350676.5:n.2238-118_2238-114dup
ENST00000396282.6:c.1841-118_1841-114dup
ENST00000443302.5:c.1420-118_1420-114dup
ENST00000615775.4:c.557-118_557-114dup ENSP00000482159.1:n.557-118_557-114dup
NM_001184896.1:c.2238-118_2238-114dup NP_001171825.1:n.2238-118_2238-114dup
NM_001184897.1:c.1827-118_1827-114dup NP_001171826.1:n.1827-118_1827-114dup
NM_001184898.1:c.2079-118_2079-114dup NP_001171827.1:n.2079-118_2079-114dup
NM_015107.2:c.2130-118_2130-114dup NP_055922.1:n.2130-118_2130-114dup
XM_005261996.1:c.2238-118_2238-114dup XP_005262053.1:n.2238-118_2238-114dup
XM_005261997.2:c.2130-118_2130-114dup XP_005262054.1:n.2130-118_2130-114dup
XM_005261999.1:c.2130-118_2130-114dup XP_005262056.1:n.2130-118_2130-114dup
XM_005262000.1:c.1935-118_1935-114dup XP_005262057.1:n.1935-118_1935-114dup
XM_006724585.1:c.2238-118_2238-114dup XP_006724648.1:n.2238-118_2238-114dup
XM_011530778.1:c.2238-118_2238-114dup XP_011529080.1:n.2238-118_2238-114dup
XM_005261997.4:c.2130-118_2130-114dup XP_005262054.1:n.2130-118_2130-114dup
XM_017029361.2:c.2130-118_2130-114dup XP_016884850.1:n.2130-118_2130-114dup
XM_017029362.2:c.2130-118_2130-114dup XP_016884851.1:n.2130-118_2130-114dup
NM_001184898.2:c.2079-118_2079-114dup NP_001171827.1:n.2079-118_2079-114dup
NM_015107.3:c.2130-118_2130-114dup MANE Select NP_055922.1:n.2130-118_2130-114dup
NM_001184897.2:c.1827-118_1827-114dup NP_001171826.1:n.1827-118_1827-114dup