Revel Score:
ENST00000248633 (MANE Select)
0.118
ENST00000428214
0.118
ENST00000545192
0.118
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.92517794A>T , CM000669.2:g.92517794A>T | GRCh38 |
| NC_000007.13:g.92147108A>T , CM000669.1:g.92147108A>T | GRCh37 |
| NC_000007.12:g.91985044A>T | NCBI36 |
| NG_008341.1:g.15738T>A | |
| NG_008341.2:g.15738T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248633.9:c.721T>A MANE Select | ENSP00000248633.4:p.Ser241Thr | |
| ENST00000248633.8:c.721T>A | ENSP00000248633.4:p.Ser241Thr | |
| ENST00000428214.5:c.721T>A | ENSP00000394413.1:p.Ser241Thr | |
| ENST00000438045.5:c.274-3827T>A | ENSP00000410438.1:n.274-3827T>A | |
| ENST00000484913.5:n.760T>A | ||
| NM_000466.2:c.721T>A | NP_000457.1:p.Ser241Thr | |
| NM_001282677.1:c.721T>A | NP_001269606.1:p.Ser241Thr | |
| NM_001282678.1:c.97T>A | NP_001269607.1:p.Ser33Thr | |
| XR_242246.3:n.817T>A | ||
| XR_242246.5:n.768T>A | ||
| NM_000466.3:c.721T>A MANE Select | NP_000457.1:p.Ser241Thr | |
| NM_001282677.2:c.721T>A | NP_001269606.1:p.Ser241Thr | |
| NM_001282678.2:c.97T>A | NP_001269607.1:p.Ser33Thr |