Revel Score:
ENST00000542917
0.519
ENST00000267163 (MANE Select)
0.519
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48381402C>G , CM000675.2:g.48381402C>G | GRCh38 |
| NC_000013.10:g.48955538C>G , CM000675.1:g.48955538C>G | GRCh37 |
| NC_000013.9:g.47853539C>G | NCBI36 |
| NG_009009.1:g.82656C>G , LRG_517:g.82656C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.1654C>G MANE Select | ENSP00000267163.4:p.Arg552Gly | |
| ENST00000643064.1:c.153C>G | ||
| ENST00000650461.1:c.1654C>G | ENSP00000497193.1:p.Arg552Gly | |
| ENST00000267163.4:c.1654C>G | ENSP00000267163.4:p.Arg552Gly | |
| NM_000321.2:c.1654C>G , LRG_517t1:c.1654C>G | NP_000312.2:p.Arg552Gly | |
| XM_011535171.1:c.1393C>G | XP_011533473.1:p.Arg465Gly | |
| XM_011535171.2:c.1393C>G | XP_011533473.1:p.Arg465Gly | |
| NM_000321.3:c.1654C>G MANE Select | NP_000312.2:p.Arg552Gly |