Canonical Allele Identifier: CA2679279799

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.63720496_63720503del , CM000668.2:g.63720496_63720503del GRCh38
NC_000006.11:g.64430392_64430399del , CM000668.1:g.64430392_64430399del GRCh37
NC_000006.10:g.64488351_64488358del NCBI36
NG_023443.1:g.1991724_1991731del
NG_023443.2:g.1991727_1991734del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262043.8:c.*6788_*6795del (PHF3) MANE Select ENSP00000262043.4:n.*6788_*6795del
ENST00000503581.6:c.*97_*104del (EYS) MANE Select ENSP00000424243.1:n.*97_*104del
ENST00000370621.7:c.*97_*104del (EYS) ENSP00000359655.3:n.*97_*104del
ENST00000503581.5:c.*97_*104del (EYS) ENSP00000424243.1:n.*97_*104del
ENST00000505138.1:c.363+9134_363+9141del (PHF3)
NM_001142800.1:c.*97_*104del (EYS) NP_001136272.1:n.*97_*104del
NM_001292009.1:c.*97_*104del (EYS) NP_001278938.1:n.*97_*104del
NM_001142800.2:c.*97_*104del (EYS) MANE Select NP_001136272.1:n.*97_*104del
NM_001290259.2:c.*6788_*6795del (PHF3) NP_001277188.1:n.*6788_*6795del
NM_001370348.2:c.*6788_*6795del (PHF3) MANE Select NP_001357277.1:n.*6788_*6795del
NM_001370349.2:c.*6788_*6795del (PHF3) NP_001357278.1:n.*6788_*6795del
NM_001370350.2:c.*6788_*6795del (PHF3) NP_001357279.1:n.*6788_*6795del
NM_015153.4:c.*6788_*6795del (PHF3) NP_055968.1:n.*6788_*6795del
NM_001292009.2:c.*97_*104del (EYS) NP_001278938.1:n.*97_*104del