Revel Score:
ENST00000245407 (MANE Select)
0.682
ENST00000435065
0.682
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.132369975G>T , CM000667.2:g.132369975G>T | GRCh38 |
| NC_000005.9:g.131705667G>T , CM000667.1:g.131705667G>T | GRCh37 |
| NC_000005.8:g.131733566G>T | NCBI36 |
| NG_008982.1:g.5267G>T | |
| NG_008982.2:g.5272G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000415928.6:c.3G>T | ENSP00000388838.2:p.Met1Ile | |
| ENST00000435065.7:c.3G>T | ENSP00000402760.2:p.Met1Ile | |
| ENST00000448810.6:c.3G>T | ENSP00000401860.2:p.Met1Ile | |
| ENST00000686757.1:c.3G>T | ENSP00000510721.1:p.Met1Ile | |
| ENST00000687740.1:n.137G>T | ||
| ENST00000689271.1:c.3G>T | ENSP00000510797.1:p.Met1Ile | |
| ENST00000690900.1:c.3G>T | ENSP00000510703.1:p.Met1Ile | |
| ENST00000692413.1:c.3G>T | ENSP00000509374.1:p.Met1Ile | |
| ENST00000692825.1:c.3G>T | ENSP00000509447.1:p.Met1Ile | |
| ENST00000693308.1:c.3G>T | ENSP00000509770.1:p.Met1Ile | |
| ENST00000693763.1:n.137G>T | ||
| ENST00000245407.8:c.3G>T MANE Select | ENSP00000245407.3:p.Met1Ile | |
| ENST00000245407.7:c.3G>T | ENSP00000245407.3:p.Met1Ile | |
| ENST00000435065.6:c.3G>T | ENSP00000402760.2:p.Met1Ile | |
| ENST00000437841.6:c.3G>T | ENSP00000400553.1:p.Met1Ile | |
| NM_001308122.1:c.3G>T | NP_001295051.1:p.Met1Ile | |
| NM_003060.3:c.3G>T | NP_003051.1:p.Met1Ile | |
| XR_427718.1:n.272G>T | ||
| XR_948290.1:n.272G>T | ||
| XR_948291.1:n.272G>T | ||
| XR_001742215.1:n.272G>T | ||
| XR_001742216.1:n.272G>T | ||
| XR_427718.2:n.272G>T | ||
| XR_948290.2:n.272G>T | ||
| XR_948291.2:n.272G>T | ||
| NM_003060.4:c.3G>T MANE Select | NP_003051.1:p.Met1Ile | |
| NM_001308122.2:c.3G>T | NP_001295051.1:p.Met1Ile |