Revel Score:
ENST00000331163 (MANE Select)
0.281
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.39243962A>C , CM000684.2:g.39243962A>C | GRCh38 |
| NC_000022.10:g.39639967A>C , CM000684.1:g.39639967A>C | GRCh37 |
| NC_000022.9:g.37969913A>C | NCBI36 |
| NG_012111.1:g.5991T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000331163.11:c.2T>G MANE Select | ENSP00000330382.6:p.Met1Arg | |
| ENST00000331163.10:c.2T>G | ENSP00000330382.6:p.Met1Arg | |
| NM_002608.2:c.2T>G | NP_002599.1:p.Met1Arg | |
| NM_002608.3:c.2T>G | NP_002599.1:p.Met1Arg | |
| NM_002608.4:c.2T>G MANE Select | NP_002599.1:p.Met1Arg |