Canonical Allele Identifier: CA2679279787

Gene: PHF3 EYS

Linked Data

• gnomAD v4: 6-63720475-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.63720475C>A , CM000668.2:g.63720475C>A	GRCh38
NC_000006.11:g.64430371C>A , CM000668.1:g.64430371C>A	GRCh37
NC_000006.10:g.64488330C>A	NCBI36
NG_023443.1:g.1991748G>T
NG_023443.2:g.1991751G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262043.8:c.*6767C>A (PHF3) MANE Select	ENSP00000262043.4:n.*6767C>A
ENST00000503581.6:c.*121G>T (EYS) MANE Select	ENSP00000424243.1:n.*121G>T
ENST00000370621.7:c.*121G>T (EYS)	ENSP00000359655.3:n.*121G>T
ENST00000503581.5:c.*121G>T (EYS)	ENSP00000424243.1:n.*121G>T
ENST00000505138.1:c.363+9113C>A (PHF3)
NM_001142800.1:c.*121G>T (EYS)	NP_001136272.1:n.*121G>T
NM_001292009.1:c.*121G>T (EYS)	NP_001278938.1:n.*121G>T
NM_001142800.2:c.*121G>T (EYS) MANE Select	NP_001136272.1:n.*121G>T
NM_001290259.2:c.*6767C>A (PHF3)	NP_001277188.1:n.*6767C>A
NM_001370348.2:c.*6767C>A (PHF3) MANE Select	NP_001357277.1:n.*6767C>A
NM_001370349.2:c.*6767C>A (PHF3)	NP_001357278.1:n.*6767C>A
NM_001370350.2:c.*6767C>A (PHF3)	NP_001357279.1:n.*6767C>A
NM_015153.4:c.*6767C>A (PHF3)	NP_055968.1:n.*6767C>A
NM_001292009.2:c.*121G>T (EYS)	NP_001278938.1:n.*121G>T