Revel Score:
ENST00000316623 (MANE Select)
0.754
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48420698T>A , CM000677.2:g.48420698T>A | GRCh38 |
| NC_000015.9:g.48712895T>A , CM000677.1:g.48712895T>A | GRCh37 |
| NC_000015.8:g.46500187T>A | NCBI36 |
| NG_008805.2:g.230091A>T , LRG_778:g.230091A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.*616A>T | ENSP00000453958.2:n.*616A>T | |
| ENST00000674301.2:c.*1321A>T | ENSP00000501333.2:n.*1321A>T | |
| ENST00000682170.1:n.1989A>T | ||
| ENST00000682767.1:n.1105A>T | ||
| ENST00000316623.10:c.7808A>T MANE Select | ENSP00000325527.5:p.Asn2603Ile | |
| ENST00000674301.1:c.2974A>T | ENSP00000501333.1:n.2974A>T | |
| ENST00000316623.9:c.7808A>T | ENSP00000325527.5:p.Asn2603Ile | |
| ENST00000559133.5:c.3177A>T | ||
| NM_000138.4:c.7808A>T , LRG_778t1:c.7808A>T | NP_000129.3:p.Asn2603Ile | |
| NM_000138.5:c.7808A>T MANE Select | NP_000129.3:p.Asn2603Ile |