Revel Score:
ENST00000311895 (MANE Select)
0.205
ENST00000389138
0.205
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.13948132C>A , CM000678.2:g.13948132C>A | GRCh38 |
| NC_000016.9:g.14041989C>A , CM000678.1:g.14041989C>A | GRCh37 |
| NC_000016.8:g.13949490C>A | NCBI36 |
| NG_011442.1:g.32976C>A , LRG_463:g.32976C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682617.1:c.2674C>A | ENSP00000507912.1:p.Pro892Thr | |
| ENST00000683962.1:c.*2230C>A | ENSP00000506854.1:n.*2230C>A | |
| ENST00000311895.8:c.2536C>A MANE Select | ENSP00000310520.7:p.Pro846Thr | |
| ENST00000311895.7:c.2536C>A | ENSP00000310520.7:p.Pro846Thr | |
| ENST00000389138.7:n.1813C>A | ||
| NM_005236.2:c.2536C>A , LRG_463t1:c.2536C>A | NP_005227.1:p.Pro846Thr | |
| XM_011522424.1:c.2674C>A | XP_011520726.1:p.Pro892Thr | |
| XM_011522425.1:c.1993C>A | XP_011520727.1:p.Pro665Thr | |
| XM_011522426.1:c.1747C>A | XP_011520728.1:p.Pro583Thr | |
| XM_011522427.1:c.1186C>A | XP_011520729.1:p.Pro396Thr | |
| XR_932805.1:n.2695C>A | ||
| XM_011522424.3:c.2674C>A | XP_011520726.1:p.Pro892Thr | |
| XM_017023043.2:c.1747C>A | XP_016878532.1:p.Pro583Thr | |
| NM_005236.3:c.2536C>A MANE Select | NP_005227.1:p.Pro846Thr |