Revel Score:
ENST00000311907 (MANE Select)
0.930
ENST00000530231
0.930
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.46728138C>T , CM000673.2:g.46728138C>T | GRCh38 |
| NC_000011.9:g.46749688C>T , CM000673.1:g.46749688C>T | GRCh37 |
| NC_000011.8:g.46706264C>T | NCBI36 |
| NG_008953.1:g.13946C>T , LRG_551:g.13946C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311907.10:c.1273C>T MANE Select | ENSP00000308541.5:p.Arg425Cys | |
| ENST00000311907.9:c.1273C>T | ENSP00000308541.5:p.Arg425Cys | |
| ENST00000530231.5:c.1273C>T | ENSP00000433907.1:p.Arg425Cys | |
| NM_000506.3:c.1273C>T | NP_000497.1:p.Arg425Cys | |
| NM_000506.4:c.1273C>T , LRG_551t1:c.1273C>T | NP_000497.1:p.Arg425Cys | |
| NM_001311257.1:c.1225C>T | NP_001298186.1:p.Arg409Cys | |
| XR_428840.2:n.1317C>T | ||
| XR_428840.4:n.1308C>T | ||
| NM_000506.5:c.1273C>T MANE Select | NP_000497.1:p.Arg425Cys | |
| NM_001311257.2:c.1225C>T | NP_001298186.1:p.Arg409Cys |