Revel Score:
ENST00000155840 (MANE Select)
0.713
ENST00000335475
0.713
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2583466A>G , CM000673.2:g.2583466A>G | GRCh38 |
| NC_000011.9:g.2604696A>G , CM000673.1:g.2604696A>G | GRCh37 |
| NC_000011.8:g.2561272A>G | NCBI36 |
| NG_008935.1:g.143476A>G , LRG_287:g.143476A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496887.7:c.692A>G | ENSP00000434560.2:p.Lys231Arg | |
| ENST00000646564.2:c.509A>G | ENSP00000495806.2:p.Lys170Arg | |
| ENST00000155840.12:c.953A>G MANE Select | ENSP00000155840.2:p.Lys318Arg | |
| ENST00000335475.6:c.572A>G | ENSP00000334497.5:p.Lys191Arg | |
| ENST00000646564.1:c.155A>G | ENSP00000495806.1:p.Lys52Arg | |
| ENST00000155840.9:c.953A>G | ENSP00000155840.2:p.Lys318Arg | |
| ENST00000335475.5:c.572A>G | ENSP00000334497.5:p.Lys191Arg | |
| NM_000218.2:c.953A>G , LRG_287t1:c.953A>G | NP_000209.2:p.Lys318Arg | |
| NM_181798.1:c.572A>G , LRG_287t2:c.572A>G | NP_861463.1:p.Lys191Arg | |
| NM_000218.3:c.953A>G MANE Select | NP_000209.2:p.Lys318Arg |