Revel Score:
ENST00000316623 (MANE Select)
0.962
ENST00000389087
0.962
ENST00000544030
0.962
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48446706C>A , CM000677.2:g.48446706C>A | GRCh38 |
| NC_000015.9:g.48738903C>A , CM000677.1:g.48738903C>A | GRCh37 |
| NC_000015.8:g.46526195C>A | NCBI36 |
| NG_008805.2:g.204083G>T , LRG_778:g.204083G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.5788G>T | ENSP00000453958.2:p.Asp1930Tyr | |
| ENST00000674301.2:c.5788G>T | ENSP00000501333.2:p.Asp1930Tyr | |
| ENST00000684448.1:n.4462G>T | ||
| ENST00000316623.10:c.5788G>T MANE Select | ENSP00000325527.5:p.Asp1930Tyr | |
| ENST00000674301.1:c.787G>T | ENSP00000501333.1:p.Asp263Tyr | |
| ENST00000316623.9:c.5788G>T | ENSP00000325527.5:p.Asp1930Tyr | |
| ENST00000537463.6:c.*1551G>T | ENSP00000440294.2:n.*1551G>T | |
| ENST00000559133.5:c.1095G>T | ||
| NM_000138.4:c.5788G>T , LRG_778t1:c.5788G>T | NP_000129.3:p.Asp1930Tyr | |
| NM_000138.5:c.5788G>T MANE Select | NP_000129.3:p.Asp1930Tyr |