Revel Score:
ENST00000303115 (MANE Select)
0.812
ENST00000343305
0.812
ENST00000506850
0.812
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.35871070C>G , CM000667.2:g.35871070C>G | GRCh38 |
| NC_000005.9:g.35871172C>G , CM000667.1:g.35871172C>G | GRCh37 |
| NC_000005.8:g.35906929C>G | NCBI36 |
| NG_009567.1:g.19182C>G , LRG_74:g.19182C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303115.8:c.394C>G MANE Select | ENSP00000306157.3:p.Pro132Ala | |
| ENST00000303115.7:c.394C>G | ENSP00000306157.3:p.Pro132Ala | |
| ENST00000506850.5:c.394C>G | ENSP00000421207.1:p.Pro132Ala | |
| ENST00000514217.5:c.394C>G | ENSP00000427688.1:p.Pro132Ala | |
| NM_002185.3:c.394C>G | NP_002176.2:p.Pro132Ala | |
| NR_120485.1:n.497C>G | ||
| XM_005248299.2:c.394C>G | XP_005248356.1:p.Pro132Ala | |
| XM_005248300.1:c.394C>G | XP_005248357.1:p.Pro132Ala | |
| XM_011514037.1:c.394C>G | XP_011512339.1:p.Pro132Ala | |
| NM_002185.4:c.394C>G | NP_002176.2:p.Pro132Ala | |
| NR_120485.2:n.523C>G | ||
| XM_005248299.4:c.394C>G | XP_005248356.1:p.Pro132Ala | |
| NM_002185.5:c.394C>G MANE Select | NP_002176.2:p.Pro132Ala | |
| NR_120485.3:n.481C>G |