Revel Score:
ENST00000306077 (MANE Select)
0.181
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.14141752T>G , CM000665.2:g.14141752T>G | GRCh38 |
| NC_000003.11:g.14183252T>G , CM000665.1:g.14183252T>G | GRCh37 |
| NC_000003.10:g.14158253T>G | NCBI36 |
| NG_008975.1:g.21813T>G , LRG_435:g.21813T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000432444.2:c.*1190T>G | ENSP00000395617.1:n.*1190T>G | |
| ENST00000306077.5:c.1160T>G MANE Select | ENSP00000303992.5:p.Ile387Ser | |
| ENST00000306077.4:c.1160T>G | ENSP00000303992.4:p.Ile387Ser | |
| ENST00000601399.3:n.327+2455T>G | ||
| ENST00000608606.1:c.236+2455T>G | ||
| ENST00000626721.1:n.25T>G | ||
| NM_024334.2:c.1160T>G , LRG_435t1:c.1160T>G | NP_077310.1:p.Ile387Ser | |
| XM_011534109.1:c.1055T>G | XP_011532411.1:p.Ile352Ser | |
| XM_017007176.2:c.1055T>G | XP_016862665.1:p.Ile352Ser | |
| NM_024334.3:c.1160T>G MANE Select | NP_077310.1:p.Ile387Ser |