Revel Score:
ENST00000366684 (MANE Select)
0.887
ENST00000366682
0.887
ENST00000342787
0.887
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.229432597A>T , CM000663.2:g.229432597A>T | GRCh38 |
| NC_000001.10:g.229568344A>T , CM000663.1:g.229568344A>T | GRCh37 |
| NC_000001.9:g.227634967A>T | NCBI36 |
| NG_006672.1:g.6500T>A , LRG_429:g.6500T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366683.4:c.413T>A | ENSP00000355644.4:p.Ile138Asn | |
| ENST00000684723.1:c.278T>A | ENSP00000508084.1:p.Ile93Asn | |
| ENST00000366683.3:c.413T>A | ENSP00000355644.3:p.Ile138Asn | |
| ENST00000366684.7:c.413T>A MANE Select | ENSP00000355645.3:p.Ile138Asn | |
| NM_001100.3:c.413T>A , LRG_429t1:c.413T>A | NP_001091.1:p.Ile138Asn | |
| NM_001100.4:c.413T>A MANE Select | NP_001091.1:p.Ile138Asn |