Revel Score:
ENST00000302850 (MANE Select)
0.973
ENST00000341500
0.973
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7125437C>A , CM000681.2:g.7125437C>A | GRCh38 |
| NC_000019.9:g.7125448C>A , CM000681.1:g.7125448C>A | GRCh37 |
| NC_000019.8:g.7076448C>A | NCBI36 |
| NG_008852.2:g.173564G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000302850.10:c.3104G>T MANE Select | ENSP00000303830.4:p.Gly1035Val | |
| ENST00000302850.9:c.3104G>T | ENSP00000303830.4:p.Gly1035Val | |
| ENST00000341500.9:c.3068G>T | ENSP00000342838.4:p.Gly1023Val | |
| NM_000208.2:c.3104G>T | NP_000199.2:p.Gly1035Val | |
| NM_000208.3:c.3104G>T | NP_000199.2:p.Gly1035Val | |
| NM_001079817.1:c.3068G>T | NP_001073285.1:p.Gly1023Val | |
| NM_001079817.2:c.3068G>T | NP_001073285.1:p.Gly1023Val | |
| XM_011527988.1:c.3179G>T | XP_011526290.1:p.Gly1060Val | |
| XM_011527989.1:c.3143G>T | XP_011526291.1:p.Gly1048Val | |
| XM_011527988.2:c.3101G>T | XP_011526290.2:p.Gly1034Val | |
| XM_011527989.3:c.3065G>T | XP_011526291.2:p.Gly1022Val | |
| NM_000208.4:c.3104G>T MANE Select | NP_000199.2:p.Gly1035Val | |
| NM_001079817.3:c.3068G>T | NP_001073285.1:p.Gly1023Val |