Revel Score:
ENST00000264932 (MANE Select)
0.704
ENST00000327872
0.704
ENST00000504309
0.704
ENST00000510361
0.704
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.236518C>T , CM000667.2:g.236518C>T | GRCh38 |
| NC_000005.9:g.236633C>T , CM000667.1:g.236633C>T | GRCh37 |
| NC_000005.8:g.289633C>T | NCBI36 |
| NG_012339.1:g.23278C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264932.11:c.1351C>T MANE Select | ENSP00000264932.6:p.Arg451Cys | |
| ENST00000651543.1:c.*84C>T | ENSP00000499215.1:n.*84C>T | |
| ENST00000264932.10:c.1351C>T | ENSP00000264932.6:p.Arg451Cys | |
| ENST00000504309.5:c.1351C>T | ENSP00000426514.1:p.Arg451Cys | |
| ENST00000505555.5:n.1391C>T | ||
| ENST00000510361.5:c.1207C>T | ENSP00000427703.1:p.Arg403Cys | |
| ENST00000511810.5:n.2098C>T | ||
| ENST00000514027.5:n.1306C>T | ||
| ENST00000515752.5:n.937C>T | ||
| ENST00000515815.5:c.6C>T | ||
| ENST00000617470.4:c.916C>T | ENSP00000484230.1:p.Arg306Cys | |
| NM_001294332.1:c.1207C>T | NP_001281261.1:p.Arg403Cys | |
| NM_004168.3:c.1351C>T | NP_004159.2:p.Arg451Cys | |
| XM_005248331.2:c.1351C>T | XP_005248388.1:p.Arg451Cys | |
| XM_011514072.1:c.1351C>T | XP_011512374.1:p.Arg451Cys | |
| XM_011514073.1:c.1351C>T | XP_011512375.1:p.Arg451Cys | |
| XR_925638.1:n.1484C>T | ||
| NM_001330758.1:c.1351C>T | NP_001317687.1:p.Arg451Cys | |
| XM_011514072.2:c.1351C>T | XP_011512374.1:p.Arg451Cys | |
| XM_011514073.2:c.1351C>T | XP_011512375.1:p.Arg451Cys | |
| XM_017009685.2:c.1351C>T | XP_016865174.1:p.Arg451Cys | |
| XM_024446143.1:c.1207C>T | XP_024301911.1:p.Arg403Cys | |
| XR_002956167.1:n.1398C>T | ||
| NM_004168.4:c.1351C>T MANE Select | NP_004159.2:p.Arg451Cys | |
| NM_001294332.2:c.1207C>T | NP_001281261.1:p.Arg403Cys | |
| NM_001330758.2:c.1351C>T | NP_001317687.1:p.Arg451Cys |