Revel Score:
ENST00000380794
0.328
ENST00000405623
0.328
ENST00000264708
0.328
ENST00000395826 (MANE Select)
0.328
ENST00000449220
0.328
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.25161744G>C , CM000664.2:g.25161744G>C | GRCh38 |
| NC_000002.11:g.25384613G>C , CM000664.1:g.25384613G>C | GRCh37 |
| NC_000002.10:g.25238117G>C | NCBI36 |
| NG_008997.1:g.11947C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395826.7:c.141C>G MANE Select | ENSP00000379170.2:p.Ile47Met | |
| ENST00000264708.7:c.141C>G | ENSP00000264708.3:p.Ile47Met | |
| ENST00000380794.5:c.141C>G | ENSP00000370171.1:p.Ile47Met | |
| ENST00000395826.6:c.141C>G | ENSP00000379170.2:p.Ile47Met | |
| ENST00000405623.5:c.141C>G | ENSP00000384092.1:p.Ile47Met | |
| ENST00000449220.1:c.141C>G | ENSP00000387993.1:p.Ile47Met | |
| NM_000939.2:c.141C>G | NP_000930.1:p.Ile47Met | |
| NM_001035256.1:c.141C>G | NP_001030333.1:p.Ile47Met | |
| XM_011532917.1:c.141C>G | XP_011531219.1:p.Ile47Met | |
| NM_000939.3:c.141C>G | NP_000930.1:p.Ile47Met | |
| NM_001035256.2:c.141C>G | NP_001030333.1:p.Ile47Met | |
| NM_001319204.1:c.141C>G | NP_001306133.1:p.Ile47Met | |
| NM_001319205.1:c.141C>G | NP_001306134.1:p.Ile47Met | |
| NM_000939.4:c.141C>G MANE Select | NP_000930.1:p.Ile47Met | |
| NM_001319204.2:c.141C>G | NP_001306133.1:p.Ile47Met | |
| NM_001319205.2:c.141C>G | NP_001306134.1:p.Ile47Met | |
| NM_001035256.3:c.141C>G | NP_001030333.1:p.Ile47Met |