Revel Score:
ENST00000372213 (MANE Select)
0.978
ENST00000372206
0.978
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.80274599C>G , CM000672.2:g.80274599C>G | GRCh38 |
| NC_000010.10:g.82034355C>G , CM000672.1:g.82034355C>G | GRCh37 |
| NC_000010.9:g.82024335C>G | NCBI36 |
| NG_008083.1:g.20080G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372213.8:c.1006G>C MANE Select | ENSP00000361287.3:p.Gly336Arg | |
| ENST00000372213.7:c.1006G>C | ENSP00000361287.3:p.Gly336Arg | |
| ENST00000480845.1:n.238G>C | ||
| ENST00000485270.5:n.518G>C | ||
| NM_000429.2:c.1006G>C | NP_000420.1:p.Gly336Arg | |
| XM_005269842.3:c.1006G>C | XP_005269899.1:p.Gly336Arg | |
| XM_005269843.3:c.883G>C | XP_005269900.1:p.Gly295Arg | |
| NM_000429.3:c.1006G>C MANE Select | NP_000420.1:p.Gly336Arg |