Revel Score:
ENST00000405093 (MANE Select)
0.815
ENST00000356287
0.815
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23394294A>T , CM000676.2:g.23394294A>T | GRCh38 |
| NC_000014.8:g.23863503A>T , CM000676.1:g.23863503A>T | GRCh37 |
| NC_000014.7:g.22933343A>T | NCBI36 |
| NG_023444.1:g.18984T>A , LRG_389:g.18984T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000405093.9:c.2459T>A MANE Select | ENSP00000386041.3:p.Ile820Asn | |
| ENST00000356287.3:c.2459T>A | ENSP00000348634.3:p.Ile820Asn | |
| ENST00000405093.7:c.2459T>A | ENSP00000386041.3:p.Ile820Asn | |
| NM_002471.3:c.2459T>A , LRG_389t1:c.2459T>A | NP_002462.2:p.Ile820Asn | |
| NM_002471.4:c.2459T>A MANE Select | NP_002462.2:p.Ile820Asn |