Revel Score:
ENST00000442011 (MANE Select)
0.457
ENST00000398813
0.457
ENST00000508076
0.457
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.136062674G>T , CM000667.2:g.136062674G>T | GRCh38 |
| NC_000005.9:g.135398363G>T , CM000667.1:g.135398363G>T | GRCh37 |
| NC_000005.8:g.135426262G>T | NCBI36 |
| NG_012646.1:g.38780G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000442011.7:c.1998G>T MANE Select | ENSP00000416330.2:p.Arg666Ser | |
| ENST00000442011.6:c.1998G>T | ENSP00000416330.2:p.Arg666Ser | |
| ENST00000503087.1:c.213-512G>T | ||
| ENST00000504411.1:n.402G>T | ||
| ENST00000506699.5:n.2515G>T | ||
| ENST00000507018.5:c.1976G>T | ||
| ENST00000508076.5:c.144G>T | ENSP00000423935.1:p.Arg48Ser | |
| ENST00000514554.5:c.1059-512G>T | ||
| NM_000358.2:c.1998G>T | NP_000349.1:p.Arg666Ser | |
| NM_000358.3:c.1998G>T MANE Select | NP_000349.1:p.Arg666Ser |