Revel Score:
ENST00000339994 (MANE Select)
0.424
ENST00000528731
0.424
ClinVar RCV:
ClinVar Variation:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.17387059T>C , CM000673.2:g.17387059T>C | GRCh38 |
| NC_000011.9:g.17408606T>C , CM000673.1:g.17408606T>C | GRCh37 |
| NC_000011.8:g.17365182T>C | NCBI36 |
| NG_012446.1:g.6601A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682350.1:c.772A>G | ENSP00000508090.1:p.Thr258Ala | |
| ENST00000682764.1:c.772A>G | ENSP00000506780.1:p.Thr258Ala | |
| ENST00000339994.5:c.1033A>G MANE Select | ENSP00000345708.4:p.Thr345Ala | |
| ENST00000339994.4:c.1033A>G | ENSP00000345708.4:p.Thr345Ala | |
| ENST00000528731.1:c.772A>G | ENSP00000434755.1:p.Thr258Ala | |
| NM_000525.3:c.1033A>G | NP_000516.3:p.Thr345Ala | |
| NM_001166290.1:c.772A>G | NP_001159762.1:p.Thr258Ala | |
| XM_006718226.2:c.772A>G | XP_006718289.1:p.Thr258Ala | |
| XR_930867.1:n.1191A>G | ||
| XM_006718226.3:c.772A>G | XP_006718289.1:p.Thr258Ala | |
| XM_017017680.1:c.772A>G | XP_016873169.1:p.Thr258Ala | |
| NM_001166290.2:c.772A>G | NP_001159762.1:p.Thr258Ala | |
| NM_001377296.1:c.772A>G | NP_001364225.1:p.Thr258Ala | |
| NM_001377297.1:c.772A>G | NP_001364226.1:p.Thr258Ala | |
| NM_000525.4:c.1033A>G MANE Select | NP_000516.3:p.Thr345Ala |