Revel Score:
ENST00000395324
0.955
ENST00000229022
0.955
ENST00000549336 (MANE Select)
0.955
ENST00000550325
0.955
ENST00000535672
0.955
ENST00000546653
0.955
ENST00000550314
0.955
ENST00000548664
0.955
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.47865175C>A , CM000674.2:g.47865175C>A | GRCh38 |
| NC_000012.11:g.48258958C>A , CM000674.1:g.48258958C>A | GRCh37 |
| NC_000012.10:g.46545225C>A | NCBI36 |
| NG_008731.1:g.44857G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000229022.9:c.149G>T | ENSP00000229022.5:p.Arg50Leu | |
| ENST00000549336.6:c.149G>T MANE Select | ENSP00000449573.2:p.Arg50Leu | |
| ENST00000229022.7:c.149G>T | ENSP00000229022.3:p.Arg50Leu | |
| ENST00000395324.6:c.149G>T | ENSP00000378734.2:p.Arg50Leu | |
| ENST00000546653.5:c.149G>T | ENSP00000448659.1:p.Arg50Leu | |
| ENST00000547065.1:c.*151G>T | ENSP00000449074.1:n.*151G>T | |
| ENST00000548664.1:c.149G>T | ENSP00000450105.1:p.Arg50Leu | |
| ENST00000549336.5:c.149G>T | ENSP00000449573.1:p.Arg50Leu | |
| ENST00000550314.5:c.149G>T | ENSP00000449561.1:p.Arg50Leu | |
| ENST00000550325.5:c.299G>T | ENSP00000447173.1:p.Arg100Leu | |
| NM_000376.2:c.149G>T | NP_000367.1:p.Arg50Leu | |
| NM_001017535.1:c.149G>T | NP_001017535.1:p.Arg50Leu | |
| NM_001017536.1:c.299G>T | NP_001017536.1:p.Arg100Leu | |
| XM_006719587.2:c.149G>T | XP_006719650.1:p.Arg50Leu | |
| XM_011538720.1:c.149G>T | XP_011537022.1:p.Arg50Leu | |
| NM_001364085.1:c.149G>T | NP_001351014.1:p.Arg50Leu | |
| XM_006719587.3:c.149G>T | XP_006719650.1:p.Arg50Leu | |
| XM_011538720.2:c.149G>T | XP_011537022.1:p.Arg50Leu | |
| XM_024449178.1:c.218G>T | XP_024304946.1:p.Arg73Leu | |
| NM_000376.3:c.149G>T MANE Select | NP_000367.1:p.Arg50Leu | |
| NM_001017535.2:c.149G>T | NP_001017535.1:p.Arg50Leu | |
| NM_001017536.2:c.299G>T | NP_001017536.1:p.Arg100Leu | |
| NM_001364085.2:c.149G>T | NP_001351014.1:p.Arg50Leu | |
| NM_001374661.1:c.149G>T | NP_001361590.1:p.Arg50Leu | |
| NM_001374662.1:c.149G>T | NP_001361591.1:p.Arg50Leu |