Revel Score:
ENST00000311895 (MANE Select)
0.359
ENST00000389138
0.359
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.13948129A>T , CM000678.2:g.13948129A>T | GRCh38 |
| NC_000016.9:g.14041986A>T , CM000678.1:g.14041986A>T | GRCh37 |
| NC_000016.8:g.13949487A>T | NCBI36 |
| NG_011442.1:g.32973A>T , LRG_463:g.32973A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682617.1:c.2671A>T | ENSP00000507912.1:p.Asn891Tyr | |
| ENST00000683962.1:c.*2227A>T | ENSP00000506854.1:n.*2227A>T | |
| ENST00000311895.8:c.2533A>T MANE Select | ENSP00000310520.7:p.Asn845Tyr | |
| ENST00000311895.7:c.2533A>T | ENSP00000310520.7:p.Asn845Tyr | |
| ENST00000389138.7:n.1810A>T | ||
| NM_005236.2:c.2533A>T , LRG_463t1:c.2533A>T | NP_005227.1:p.Asn845Tyr | |
| XM_011522424.1:c.2671A>T | XP_011520726.1:p.Asn891Tyr | |
| XM_011522425.1:c.1990A>T | XP_011520727.1:p.Asn664Tyr | |
| XM_011522426.1:c.1744A>T | XP_011520728.1:p.Asn582Tyr | |
| XM_011522427.1:c.1183A>T | XP_011520729.1:p.Asn395Tyr | |
| XR_932805.1:n.2692A>T | ||
| XM_011522424.3:c.2671A>T | XP_011520726.1:p.Asn891Tyr | |
| XM_017023043.2:c.1744A>T | XP_016878532.1:p.Asn582Tyr | |
| NM_005236.3:c.2533A>T MANE Select | NP_005227.1:p.Asn845Tyr |