Revel Score:
ENST00000534663
0.771
ENST00000299440 (MANE Select)
0.771
gnomAD v2:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.36573690T>G , CM000673.2:g.36573690T>G | GRCh38 |
| NC_000011.9:g.36595240T>G , CM000673.1:g.36595240T>G | GRCh37 |
| NC_000011.8:g.36551816T>G | NCBI36 |
| NG_007528.1:g.10678T>G , LRG_98:g.10678T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000697713.1:c.386T>G | ENSP00000513411.1:p.Val129Gly | |
| ENST00000697714.1:c.386T>G | ENSP00000513412.1:p.Val129Gly | |
| ENST00000697715.1:c.386T>G | ENSP00000513413.1:p.Val129Gly | |
| ENST00000299440.6:c.386T>G MANE Select | ENSP00000299440.5:p.Val129Gly | |
| ENST00000299440.5:c.386T>G | ENSP00000299440.5:p.Val129Gly | |
| ENST00000534663.1:c.386T>G | ENSP00000434610.1:p.Val129Gly | |
| NM_000448.2:c.386T>G , LRG_98t1:c.386T>G | NP_000439.1:p.Val129Gly | |
| XM_005253041.3:c.386T>G | XP_005253098.1:p.Val129Gly | |
| XM_011520250.1:c.386T>G | XP_011518552.1:p.Val129Gly | |
| XM_011520251.1:c.386T>G | XP_011518553.1:p.Val129Gly | |
| XM_005253041.4:c.386T>G | XP_005253098.1:p.Val129Gly | |
| XM_011520250.2:c.386T>G | XP_011518552.1:p.Val129Gly | |
| NM_000448.3:c.386T>G MANE Select | NP_000439.2:p.Val129Gly | |
| NM_001377277.1:c.386T>G | NP_001364206.1:p.Val129Gly | |
| NM_001377278.1:c.386T>G | NP_001364207.1:p.Val129Gly | |
| NM_001377279.1:c.386T>G | NP_001364208.1:p.Val129Gly | |
| NM_001377280.1:c.386T>G | NP_001364209.1:p.Val129Gly |