Revel Score:
ENST00000401707 (MANE Select)
0.349
ENST00000349693
0.349
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.98148848C>T , CM000670.2:g.98148848C>T | GRCh38 |
| NC_000008.10:g.99161076C>T , CM000670.1:g.99161076C>T | GRCh37 |
| NC_000008.9:g.99230252C>T | NCBI36 |
| NG_052869.1:g.36556C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000401707.7:c.1744C>T MANE Select | ENSP00000385787.2:p.Pro582Ser | |
| ENST00000349693.3:c.1744C>T | ENSP00000339529.3:p.Pro582Ser | |
| ENST00000401707.6:c.1744C>T | ENSP00000385787.2:p.Pro582Ser | |
| NM_001145860.1:c.1744C>T | NP_001139332.1:p.Pro582Ser | |
| NM_001145861.1:c.1744C>T | NP_001139333.1:p.Pro582Ser | |
| NM_015029.2:c.1744C>T | NP_055844.2:p.Pro582Ser | |
| XM_011516800.1:c.1744C>T | XP_011515102.1:p.Pro582Ser | |
| NM_001145860.2:c.1744C>T MANE Select | NP_001139332.1:p.Pro582Ser | |
| NM_001145861.2:c.1744C>T | NP_001139333.1:p.Pro582Ser | |
| NM_015029.3:c.1744C>T | NP_055844.2:p.Pro582Ser |