Revel Score:
ENST00000360004 (MANE Select)
0.114
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32581815G>A , CM000668.2:g.32581815G>A | GRCh38 |
| NC_000006.11:g.32549592G>A , CM000668.1:g.32549592G>A | GRCh37 |
| NC_000006.10:g.32657570G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360004.6:c.394C>T MANE Select | ENSP00000353099.5:p.Pro132Ser | |
| ENST00000696610.1:c.*299C>T | ENSP00000512754.1:n.*299C>T | |
| ENST00000696611.1:n.317C>T | ||
| ENST00000696612.1:n.457C>T | ||
| ENST00000696613.1:n.372C>T | ||
| ENST00000696614.1:n.522C>T | ||
| ENST00000360004.5:c.394C>T | ENSP00000353099.5:p.Pro132Ser | |
| ENST00000611060.4:c.394C>T | ENSP00000480667.1:p.Pro132Ser | |
| NM_002124.3:c.394C>T | NP_002115.2:p.Pro132Ser | |
| NM_002124.4:c.394C>T MANE Select | NP_002115.2:p.Pro132Ser |