Revel Score:
ENST00000399402
0.581
ENST00000307363 (MANE Select)
0.581
ENST00000445488
0.581
ENST00000307377
0.581
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.33021576T>C , CM000665.2:g.33021576T>C | GRCh38 |
| NC_000003.11:g.33063068T>C , CM000665.1:g.33063068T>C | GRCh37 |
| NC_000003.10:g.33038072T>C | NCBI36 |
| NG_009005.1:g.80627A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307363.10:c.1223A>G MANE Select | ENSP00000306920.4:p.Gln408Arg | |
| ENST00000307363.9:c.1223A>G | ENSP00000306920.4:p.Gln408Arg | |
| ENST00000307377.12:c.830A>G | ENSP00000305920.8:p.Gln277Arg | |
| ENST00000399402.7:c.1133A>G | ENSP00000382333.2:p.Gln378Arg | |
| ENST00000461475.5:n.322A>G | ||
| ENST00000467571.5:n.260A>G | ||
| ENST00000473477.1:n.255A>G | ||
| ENST00000497796.5:n.475A>G | ||
| NM_000404.2:c.1223A>G | NP_000395.2:p.Gln408Arg | |
| NM_000404.3:c.1223A>G | NP_000395.2:p.Gln408Arg | |
| NM_001079811.1:c.1133A>G | NP_001073279.1:p.Gln378Arg | |
| NM_001079811.2:c.1133A>G | NP_001073279.1:p.Gln378Arg | |
| NM_001135602.1:c.830A>G | NP_001129074.1:p.Gln277Arg | |
| NM_001135602.2:c.830A>G | NP_001129074.1:p.Gln277Arg | |
| NM_001317040.1:c.1367A>G | NP_001303969.1:p.Gln456Arg | |
| XR_001740634.1:n.1543-612T>C | ||
| NM_000404.4:c.1223A>G MANE Select | NP_000395.3:p.Gln408Arg | |
| NM_001079811.3:c.1133A>G | NP_001073279.2:p.Gln378Arg | |
| NM_001135602.3:c.830A>G | NP_001129074.2:p.Gln277Arg | |
| NM_001317040.2:c.1367A>G | NP_001303969.2:p.Gln456Arg | |
| NM_001393580.1:c.1223A>G | NP_001380509.1:p.Gln408Arg |