Revel Score:
ENST00000249373 (MANE Select)
0.657
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.129210997G>T , CM000669.2:g.129210997G>T | GRCh38 |
| NC_000007.13:g.128850838G>T , CM000669.1:g.128850838G>T | GRCh37 |
| NC_000007.12:g.128638074G>T | NCBI36 |
| NG_023340.1:g.27126G>T | |
| NG_023340.2:g.27126G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000249373.8:c.1685G>T MANE Select | ENSP00000249373.3:p.Arg562Leu | |
| ENST00000655644.1:c.*1440G>T | ENSP00000499377.1:n.*1440G>T | |
| ENST00000249373.7:c.1685G>T | ENSP00000249373.3:p.Arg562Leu | |
| ENST00000462420.2:c.656G>T | ||
| ENST00000475779.1:c.74G>T | ENSP00000420749.1:p.Arg25Leu | |
| NM_005631.4:c.1685G>T | NP_005622.1:p.Arg562Leu | |
| XM_011516522.1:c.1295G>T | XP_011514824.1:p.Arg432Leu | |
| XM_024446891.1:c.1295G>T | XP_024302659.1:p.Arg432Leu | |
| NM_005631.5:c.1685G>T MANE Select | NP_005622.1:p.Arg562Leu |