Revel Score:
ENST00000307503 (MANE Select)
0.966
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240869297A>T , CM000664.2:g.240869297A>T | GRCh38 |
| NC_000002.11:g.241808714A>T , CM000664.1:g.241808714A>T | GRCh37 |
| NC_000002.10:g.241457387A>T | NCBI36 |
| NG_008005.1:g.5553A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.293A>T MANE Select | ENSP00000302620.3:p.Asp98Val | |
| ENST00000307503.3:c.293A>T | ENSP00000302620.3:p.Asp98Val | |
| ENST00000472436.1:n.313A>T | ||
| NM_000030.2:c.293A>T | NP_000021.1:p.Asp98Val | |
| XR_924060.1:n.405+936T>A | ||
| NM_000030.3:c.293A>T MANE Select | NP_000021.1:p.Asp98Val |