Revel Score:
ENST00000260630
0.058
ENST00000407341
0.058
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.38075055A>C , CM000664.2:g.38075055A>C | GRCh38 |
| NC_000002.11:g.38302198A>C , CM000664.1:g.38302198A>C | GRCh37 |
| NC_000002.10:g.38155702A>C | NCBI36 |
| NG_008386.2:g.6047T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000490576.2:c.334T>G | ENSP00000478839.2:p.Ser112Ala | |
| ENST00000610745.5:c.334T>G MANE Select | ENSP00000478561.1:p.Ser112Ala | |
| ENST00000490576.1:c.334T>G | ENSP00000478839.1:p.Ser112Ala | |
| ENST00000494864.1:c.-70-3745T>G | ENSP00000479876.1:n.-70-3745T>G | |
| ENST00000610745.4:c.334T>G | ENSP00000478561.1:p.Ser112Ala | |
| ENST00000613082.1:n.376-647T>G | ||
| ENST00000614273.1:c.334T>G | ENSP00000483678.1:p.Ser112Ala | |
| NM_000104.3:c.334T>G | NP_000095.2:p.Ser112Ala | |
| NM_000104.4:c.334T>G MANE Select | NP_000095.2:p.Ser112Ala |