Revel Score:
ENST00000297784 (MANE Select)
0.385
ENST00000340019
0.385
ENST00000396235
0.385
ENST00000537917
0.385
ENST00000538054
0.385
ENST00000542143
0.385
ENST00000396237
0.385
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.72792318C>T , CM000671.2:g.72792318C>T | GRCh38 |
| NC_000009.11:g.75407234C>T , CM000671.1:g.75407234C>T | GRCh37 |
| NC_000009.10:g.74597054C>T | NCBI36 |
| NG_008213.1:g.275518C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297784.10:c.1532C>T MANE Select | ENSP00000297784.6:p.Pro511Leu | |
| ENST00000644967.1:c.1094C>T | ENSP00000496159.1:p.Pro365Leu | |
| ENST00000645053.1:c.1094C>T | ENSP00000493838.1:p.Pro365Leu | |
| ENST00000645208.2:c.1532C>T | ENSP00000494684.1:p.Pro511Leu | |
| ENST00000645773.1:c.1406C>T | ENSP00000493698.1:p.Pro469Leu | |
| ENST00000645787.1:n.1572C>T | ||
| ENST00000646619.1:c.1094C>T | ENSP00000493726.1:p.Pro365Leu | |
| ENST00000650689.1:n.1830C>T | ||
| ENST00000651183.1:c.1094C>T | ENSP00000498723.1:p.Pro365Leu | |
| ENST00000297784.9:c.1532C>T | ENSP00000297784.5:p.Pro511Leu | |
| ENST00000340019.4:c.1532C>T | ENSP00000341433.3:p.Pro511Leu | |
| ENST00000486417.5:n.156C>T | ||
| NM_138691.2:c.1532C>T | NP_619636.2:p.Pro511Leu | |
| XM_011518213.1:c.2120C>T | XP_011516515.1:p.Pro707Leu | |
| XM_017014256.1:c.1535C>T | XP_016869745.1:p.Pro512Leu | |
| NM_138691.3:c.1532C>T MANE Select | NP_619636.2:p.Pro511Leu |