Revel Score:
ENST00000248633 (MANE Select)
0.181
ENST00000428214
0.181
ENST00000545192
0.181
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.92517784C>G , CM000669.2:g.92517784C>G | GRCh38 |
| NC_000007.13:g.92147098C>G , CM000669.1:g.92147098C>G | GRCh37 |
| NC_000007.12:g.91985034C>G | NCBI36 |
| NG_008341.1:g.15748G>C | |
| NG_008341.2:g.15748G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248633.9:c.731G>C MANE Select | ENSP00000248633.4:p.Ser244Thr | |
| ENST00000248633.8:c.731G>C | ENSP00000248633.4:p.Ser244Thr | |
| ENST00000428214.5:c.731G>C | ENSP00000394413.1:p.Ser244Thr | |
| ENST00000438045.5:c.274-3817G>C | ENSP00000410438.1:n.274-3817G>C | |
| ENST00000484913.5:n.770G>C | ||
| NM_000466.2:c.731G>C | NP_000457.1:p.Ser244Thr | |
| NM_001282677.1:c.731G>C | NP_001269606.1:p.Ser244Thr | |
| NM_001282678.1:c.107G>C | NP_001269607.1:p.Ser36Thr | |
| XR_242246.3:n.827G>C | ||
| XR_242246.5:n.778G>C | ||
| NM_000466.3:c.731G>C MANE Select | NP_000457.1:p.Ser244Thr | |
| NM_001282677.2:c.731G>C | NP_001269606.1:p.Ser244Thr | |
| NM_001282678.2:c.107G>C | NP_001269607.1:p.Ser36Thr |