Revel Score:
ENST00000553106 (MANE Select)
0.733
ENST00000307000
0.733
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102855187A>G , CM000674.2:g.102855187A>G | GRCh38 |
| NC_000012.11:g.103248965A>G , CM000674.1:g.103248965A>G | GRCh37 |
| NC_000012.10:g.101773095A>G | NCBI36 |
| NG_008690.1:g.67416T>C | |
| NG_008690.2:g.108224T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.655T>C MANE Select | ENSP00000448059.1:p.Phe219Leu | |
| ENST00000307000.7:c.640T>C | ENSP00000303500.2:p.Phe214Leu | |
| ENST00000549111.5:n.751T>C | ||
| ENST00000553106.5:c.655T>C | ENSP00000448059.1:p.Phe219Leu | |
| NM_000277.1:c.655T>C | NP_000268.1:p.Phe219Leu | |
| XM_011538422.1:c.655T>C | XP_011536724.1:p.Phe219Leu | |
| NM_000277.2:c.655T>C | NP_000268.1:p.Phe219Leu | |
| NM_001354304.1:c.655T>C | NP_001341233.1:p.Phe219Leu | |
| XM_017019370.2:c.655T>C | XP_016874859.1:p.Phe219Leu | |
| NM_000277.3:c.655T>C MANE Select | NP_000268.1:p.Phe219Leu | |
| NM_001354304.2:c.655T>C | NP_001341233.1:p.Phe219Leu |