Revel Score:
ENST00000422843 (MANE Select)
0.179
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.157181111A>T , CM000667.2:g.157181111A>T | GRCh38 |
| NC_000005.9:g.156608122A>T , CM000667.1:g.156608122A>T | GRCh37 |
| NC_000005.8:g.156540700A>T | NCBI36 |
| NG_016276.1:g.5216A>T , LRG_189:g.5216A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696962.1:c.134A>T | ENSP00000513001.1:p.His45Leu | |
| ENST00000422843.8:c.134A>T MANE Select | ENSP00000398655.4:p.His45Leu | |
| ENST00000422843.7:c.134A>T | ENSP00000398655.3:p.His45Leu | |
| ENST00000517779.1:c.134A>T | ENSP00000431054.1:p.His45Leu | |
| ENST00000519402.5:n.269A>T | ||
| ENST00000520555.5:n.272A>T | ||
| ENST00000521769.5:c.-238+14965A>T | ENSP00000430327.1:n.-238+14965A>T | |
| ENST00000522616.1:n.275A>T | ||
| NM_005546.3:c.134A>T , LRG_189t1:c.134A>T | NP_005537.3:p.His45Leu | |
| NM_005546.4:c.134A>T MANE Select | NP_005537.3:p.His45Leu |