Revel Score:
ENST00000362032 (MANE Select)
0.432
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.151881290C>A , CM000665.2:g.151881290C>A | GRCh38 |
| NC_000003.11:g.151599078C>A , CM000665.1:g.151599078C>A | GRCh37 |
| NC_000003.10:g.153081768C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000362032.6:c.747C>A (SUCNR1) MANE Select | ENSP00000355156.4:p.His249Gln | |
| NM_033050.4:c.747C>A (SUCNR1) | NP_149039.2:p.His249Gln | |
| NR_110202.1:n.319+46567G>T (AADACL2-AS1) | ||
| NR_110203.1:n.319+46567G>T (AADACL2-AS1) | ||
| NM_033050.5:c.747C>A (SUCNR1) | NP_149039.2:p.His249Gln | |
| NM_033050.6:c.747C>A (SUCNR1) MANE Select | NP_149039.2:p.His249Gln |