Revel Score:
ENST00000271588 (MANE Select)
0.114
ENST00000367492
0.114
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186095386G>A , CM000663.2:g.186095386G>A | GRCh38 |
| NC_000001.10:g.186064518G>A , CM000663.1:g.186064518G>A | GRCh37 |
| NC_000001.9:g.184331141G>A | NCBI36 |
| NG_011841.1:g.365836G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271588.9:c.10438G>A MANE Select | ENSP00000271588.4:p.Ala3480Thr | |
| ENST00000271588.8:c.10438G>A | ENSP00000271588.4:p.Ala3480Thr | |
| NM_031935.2:c.10438G>A | NP_114141.2:p.Ala3480Thr | |
| XM_011510037.1:c.10153G>A | XP_011508339.1:p.Ala3385Thr | |
| XM_011510038.1:c.10438G>A | XP_011508340.1:p.Ala3480Thr | |
| XM_011510039.1:c.10438G>A | XP_011508341.1:p.Ala3480Thr | |
| XM_011510040.1:c.*86G>A | XP_011508342.1:n.*86G>A | |
| XM_011510038.3:c.10438G>A | XP_011508340.1:p.Ala3480Thr | |
| XM_017002437.1:c.8461G>A | XP_016857926.1:p.Ala2821Thr | |
| XM_024450118.1:c.*86G>A | XP_024305886.1:n.*86G>A | |
| NM_031935.3:c.10438G>A MANE Select | NP_114141.2:p.Ala3480Thr |