Revel Score:
ENST00000221996 (MANE Select)
0.748
ENST00000539067
0.748
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.47839964G>T , CM000681.2:g.47839964G>T | GRCh38 |
| NC_000019.9:g.48343221G>T , CM000681.1:g.48343221G>T | GRCh37 |
| NC_000019.8:g.53035033G>T | NCBI36 |
| NG_008605.1:g.23123G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000221996.12:c.897G>T MANE Select | ENSP00000221996.5:p.Leu299Phe | |
| ENST00000221996.11:c.897G>T | ENSP00000221996.5:p.Leu299Phe | |
| ENST00000539067.5:c.897G>T | ENSP00000445565.1:p.Leu299Phe | |
| ENST00000613299.1:c.*619G>T | ENSP00000478106.1:n.*619G>T | |
| NM_000554.4:c.897G>T | NP_000545.1:p.Leu299Phe | |
| NM_000554.5:c.897G>T | NP_000545.1:p.Leu299Phe | |
| NM_000554.6:c.897G>T MANE Select | NP_000545.1:p.Leu299Phe |