Revel Score:
ENST00000345060 (MANE Select)
0.096
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37965670G>C , CM000670.2:g.37965670G>C | GRCh38 |
| NC_000008.10:g.37823188G>C , CM000670.1:g.37823188G>C | GRCh37 |
| NC_000008.9:g.37942345G>C | NCBI36 |
| NG_011936.1:g.5997C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000345060.5:c.800C>G MANE Select | ENSP00000343782.3:p.Ala267Gly | |
| ENST00000520341.2:n.928C>G | ||
| ENST00000647937.1:c.284C>G | ENSP00000497740.1:p.Ala95Gly | |
| ENST00000345060.4:c.800C>G | ENSP00000343782.3:p.Ala267Gly | |
| ENST00000520341.1:n.75C>G | ||
| ENST00000614635.1:c.800C>G | ENSP00000480325.1:p.Ala267Gly | |
| NM_000025.2:c.800C>G | NP_000016.1:p.Ala267Gly | |
| NM_000025.3:c.800C>G MANE Select | NP_000016.1:p.Ala267Gly |