ClinGen Evidence Repository:
Classification
Likely Pathogenic
Condition
phenylketonuria
VCEP
Phenylketonuria VCEP
Revel Score:
ENST00000553106 (MANE Select)
0.849
ENST00000307000
0.849
gnomAD v2:
gnomAD v4:
ClinVar Allele:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102843715T>C , CM000674.2:g.102843715T>C | GRCh38 |
| NC_000012.11:g.103237493T>C , CM000674.1:g.103237493T>C | GRCh37 |
| NC_000012.10:g.101761623T>C | NCBI36 |
| NG_008690.1:g.78888A>G | |
| NG_008690.2:g.119696A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.1130A>G MANE Select | ENSP00000448059.1:p.Tyr377Cys | |
| ENST00000307000.7:c.1115A>G | ENSP00000303500.2:p.Tyr372Cys | |
| ENST00000549247.6:n.889A>G | ||
| ENST00000551114.2:n.792A>G | ||
| ENST00000553106.5:c.1130A>G | ENSP00000448059.1:p.Tyr377Cys | |
| ENST00000635477.1:c.234A>G | ||
| ENST00000635528.1:n.645A>G | ||
| NM_000277.1:c.1130A>G | NP_000268.1:p.Tyr377Cys | |
| XM_011538422.1:c.1073A>G | XP_011536724.1:p.Tyr358Cys | |
| NM_000277.2:c.1130A>G | NP_000268.1:p.Tyr377Cys | |
| NM_001354304.1:c.1130A>G | NP_001341233.1:p.Tyr377Cys | |
| NM_000277.3:c.1130A>G MANE Select | NP_000268.1:p.Tyr377Cys | |
| NM_001354304.2:c.1130A>G | NP_001341233.1:p.Tyr377Cys |