Revel Score:
ENST00000296820
0.273
ENST00000508104
0.273
ENST00000310581 (MANE Select)
0.638
ENST00000334602
0.638
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1266519C>A , CM000667.2:g.1266519C>A | GRCh38 |
| NC_000005.9:g.1266634C>A , CM000667.1:g.1266634C>A | GRCh37 |
| NC_000005.8:g.1319634C>A | NCBI36 |
| NG_009265.1:g.33529G>T , LRG_343:g.33529G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000310581.10:c.2599G>T MANE Select | ENSP00000309572.5:p.Val867Leu | |
| ENST00000656021.1:c.*2145G>T | ENSP00000499759.1:n.*2145G>T | |
| ENST00000310581.9:c.2599G>T | ENSP00000309572.5:p.Val867Leu | |
| ENST00000334602.10:c.2599G>T | ENSP00000334346.6:p.Val867Leu | |
| ENST00000460137.6:c.2381G>T | ENSP00000425003.1:p.Gly794Val | |
| ENST00000484238.6:n.1230G>T | ||
| ENST00000503656.1:n.6G>T | ||
| ENST00000508104.2:c.2417G>T | ENSP00000426042.2:p.Gly806Val | |
| NM_001193376.1:c.2599G>T | NP_001180305.1:p.Val867Leu | |
| NM_198253.2:c.2599G>T , LRG_343t1:c.2599G>T | NP_937983.2:p.Val867Leu | |
| XM_011514104.1:c.1069G>T | XP_011512406.1:p.Val357Leu | |
| XM_011514105.1:c.955G>T | XP_011512407.1:p.Val319Leu | |
| XM_011514106.1:c.955G>T | XP_011512408.1:p.Val319Leu | |
| NR_149162.1:n.2475G>T | ||
| NR_149163.1:n.2439G>T | ||
| NM_001193376.2:c.2599G>T | NP_001180305.1:p.Val867Leu | |
| NM_198253.3:c.2599G>T MANE Select | NP_937983.2:p.Val867Leu | |
| NR_149162.2:n.2496G>T | ||
| NR_149163.2:n.2460G>T | ||
| NM_001193376.3:c.2599G>T | NP_001180305.1:p.Val867Leu | |
| NR_149162.3:n.2496G>T | ||
| NR_149163.3:n.2460G>T |