Canonical Allele Identifier: CA2771457330

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.63721559_63721560del , CM000668.2:g.63721559_63721560del GRCh38
NC_000006.11:g.64431455_64431456del , CM000668.1:g.64431455_64431456del GRCh37
NC_000006.10:g.64489414_64489415del NCBI36
NG_023443.1:g.1990664_1990665del
NG_023443.2:g.1990667_1990668del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262043.8:c.*7851_*7852del (PHF3) MANE Select ENSP00000262043.4:n.*7851_*7852del
ENST00000503581.6:c.8472_8473del (EYS) MANE Select ENSP00000424243.1:p.Gly2825SerfsTer15
ENST00000370616.6:c.8535_8536del (EYS) ENSP00000359650.2:p.Gly2846SerfsTer15
ENST00000370618.7:c.8472_8473del (EYS) ENSP00000359652.4:p.Gly2825SerfsTer15
ENST00000370621.7:c.8535_8536del (EYS) ENSP00000359655.3:p.Gly2846SerfsTer15
ENST00000503581.5:c.8472_8473del (EYS) ENSP00000424243.1:p.Gly2825SerfsTer15
ENST00000505138.1:c.363+10197_363+10198del (PHF3)
NM_001142800.1:c.8472_8473del (EYS) NP_001136272.1:p.Gly2825SerfsTer15
NM_001292009.1:c.8535_8536del (EYS) NP_001278938.1:p.Gly2846SerfsTer15
NM_001142800.2:c.8472_8473del (EYS) MANE Select NP_001136272.1:p.Gly2825SerfsTer15
NM_001290259.2:c.*7851_*7852del (PHF3) NP_001277188.1:n.*7851_*7852del
NM_001370348.2:c.*7851_*7852del (PHF3) MANE Select NP_001357277.1:n.*7851_*7852del
NM_001370349.2:c.*7851_*7852del (PHF3) NP_001357278.1:n.*7851_*7852del
NM_001370350.2:c.*7851_*7852del (PHF3) NP_001357279.1:n.*7851_*7852del
NM_015153.4:c.*7851_*7852del (PHF3) NP_055968.1:n.*7851_*7852del
NM_001292009.2:c.8535_8536del (EYS) NP_001278938.1:p.Gly2846SerfsTer15