Canonical Allele Identifier: CA1633381821

Gene: PHF3 EYS

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.63721375_63721383delinsTTCTGCATG , CM000668.2:g.63721375_63721383delinsTTCTGCATG	GRCh38
NC_000006.11:g.64431271_64431279delinsTTCTGCATG , CM000668.1:g.64431271_64431279delinsTTCTGCATG	GRCh37
NC_000006.10:g.64489230_64489238delinsTTCTGCATG	NCBI36
NG_023443.1:g.1990840_1990848delinsCATGCAGAA
NG_023443.2:g.1990843_1990851delinsCATGCAGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262043.8:c.*7667_*7675delinsTTCTGCATG (PHF3) MANE Select	ENSP00000262043.4:n.*7667_*7675delinsTTCTGCATG
ENST00000503581.6:c.8648_8656delinsCATGCAGAA (EYS) MANE Select	ENSP00000424243.1:p.Thr2883=
ENST00000370616.6:c.8711_8719delinsCATGCAGAA (EYS)	ENSP00000359650.2:p.Thr2904=
ENST00000370618.7:c.8648_8656delinsCATGCAGAA (EYS)	ENSP00000359652.4:p.Thr2883=
ENST00000370621.7:c.8711_8719delinsCATGCAGAA (EYS)	ENSP00000359655.3:p.Thr2904=
ENST00000503581.5:c.8648_8656delinsCATGCAGAA (EYS)	ENSP00000424243.1:p.Thr2883=
ENST00000505138.1:c.363+10013_363+10021delinsTTCTGCATG (PHF3)
NM_001142800.1:c.8648_8656delinsCATGCAGAA (EYS)	NP_001136272.1:p.Thr2883=
NM_001292009.1:c.8711_8719delinsCATGCAGAA (EYS)	NP_001278938.1:p.Thr2904=
NM_001142800.2:c.8648_8656delinsCATGCAGAA (EYS) MANE Select	NP_001136272.1:p.Thr2883=
NM_001290259.2:c.*7667_*7675delinsTTCTGCATG (PHF3)	NP_001277188.1:n.*7667_*7675delinsTTCTGCATG
NM_001370348.2:c.*7667_*7675delinsTTCTGCATG (PHF3) MANE Select	NP_001357277.1:n.*7667_*7675delinsTTCTGCATG
NM_001370349.2:c.*7667_*7675delinsTTCTGCATG (PHF3)	NP_001357278.1:n.*7667_*7675delinsTTCTGCATG
NM_001370350.2:c.*7667_*7675delinsTTCTGCATG (PHF3)	NP_001357279.1:n.*7667_*7675delinsTTCTGCATG
NM_015153.4:c.*7667_*7675delinsTTCTGCATG (PHF3)	NP_055968.1:n.*7667_*7675delinsTTCTGCATG
NM_001292009.2:c.8711_8719delinsCATGCAGAA (EYS)	NP_001278938.1:p.Thr2904=