Revel Score:
ENST00000270142 (MANE Select)
0.956
ENST00000389995
0.956
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.31668568T>G , CM000683.2:g.31668568T>G | GRCh38 |
| NC_000021.8:g.33040881T>G , CM000683.1:g.33040881T>G | GRCh37 |
| NC_000021.7:g.31962752T>G | NCBI36 |
| NG_008689.1:g.13947T>G , LRG_652:g.13947T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270142.11:c.455T>G MANE Select | ENSP00000270142.7:p.Ile152Ser | |
| ENST00000270142.10:c.455T>G | ENSP00000270142.6:p.Ile152Ser | |
| ENST00000389995.4:c.398T>G | ENSP00000374645.4:p.Ile133Ser | |
| ENST00000470944.1:n.1383T>G | ||
| NM_000454.4:c.455T>G , LRG_652t1:c.455T>G | NP_000445.1:p.Ile152Ser | |
| NM_000454.5:c.455T>G MANE Select | NP_000445.1:p.Ile152Ser |