Revel Score:
ENST00000438045
0.562
ENST00000248633 (MANE Select)
0.562
ENST00000428214
0.562
ENST00000541751
0.562
ENST00000545192
0.562
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.92506312G>C , CM000669.2:g.92506312G>C | GRCh38 |
| NC_000007.13:g.92135626G>C , CM000669.1:g.92135626G>C | GRCh37 |
| NC_000007.12:g.91973562G>C | NCBI36 |
| NG_008341.1:g.27220C>G | |
| NG_008341.2:g.27220C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248633.9:c.1836C>G MANE Select | ENSP00000248633.4:p.Ile612Met | |
| ENST00000248633.8:c.1836C>G | ENSP00000248633.4:p.Ile612Met | |
| ENST00000422866.1:c.654C>G | ||
| ENST00000428214.5:c.1836C>G | ENSP00000394413.1:p.Ile612Met | |
| ENST00000438045.5:c.870C>G | ENSP00000410438.1:p.Ile290Met | |
| ENST00000484913.5:n.1875C>G | ||
| ENST00000496420.5:n.1512C>G | ||
| NM_000466.2:c.1836C>G | NP_000457.1:p.Ile612Met | |
| NM_001282677.1:c.1836C>G | NP_001269606.1:p.Ile612Met | |
| NM_001282678.1:c.1212C>G | NP_001269607.1:p.Ile404Met | |
| XM_005250433.3:c.87C>G | XP_005250490.1:p.Ile29Met | |
| XR_242246.3:n.1932C>G | ||
| XM_017012319.2:c.87C>G | XP_016867808.1:p.Ile29Met | |
| XR_001744808.2:n.863C>G | ||
| XR_242246.5:n.1883C>G | ||
| NM_000466.3:c.1836C>G MANE Select | NP_000457.1:p.Ile612Met | |
| NM_001282677.2:c.1836C>G | NP_001269606.1:p.Ile612Met | |
| NM_001282678.2:c.1212C>G | NP_001269607.1:p.Ile404Met |