Revel Score:
ENST00000520113 (MANE Select)
0.901
ENST00000369538
0.901
ENST00000353928
0.901
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.114677986C>G , CM000663.2:g.114677986C>G | GRCh38 |
| NC_000001.10:g.115220607C>G , CM000663.1:g.115220607C>G | GRCh37 |
| NC_000001.9:g.115022130C>G | NCBI36 |
| NG_008012.1:g.22570G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369538.4:c.1136G>C | ENSP00000358551.4:p.Gly379Ala | |
| ENST00000520113.7:c.1148G>C MANE Select | ENSP00000430075.3:p.Gly383Ala | |
| ENST00000637080.1:c.931G>C | ENSP00000489753.1:n.931G>C | |
| ENST00000639077.1:n.813G>C | ||
| ENST00000369538.3:c.1235G>C | ENSP00000358551.3:p.Gly412Ala | |
| ENST00000520113.6:c.1247G>C | ENSP00000430075.2:p.Gly416Ala | |
| NM_000036.2:c.1247G>C | NP_000027.2:p.Gly416Ala | |
| NM_001172626.1:c.1235G>C | NP_001166097.1:p.Gly412Ala | |
| NM_000036.3:c.1148G>C MANE Select | NP_000027.3:p.Gly383Ala | |
| NM_001172626.2:c.1136G>C | NP_001166097.2:p.Gly379Ala |