Revel Score:
ENST00000324071 (MANE Select)
0.786
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.41006968T>G , CM000681.2:g.41006968T>G | GRCh38 |
| NC_000019.9:g.41512873T>G , CM000681.1:g.41512873T>G | GRCh37 |
| NC_000019.8:g.46204713T>G | NCBI36 |
| NG_007929.1:g.20670T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000324071.10:c.548T>G MANE Select | ENSP00000324648.2:p.Val183Gly | |
| ENST00000598834.2:c.450T>G | ||
| ENST00000324071.8:c.548T>G | ENSP00000324648.2:p.Val183Gly | |
| ENST00000593831.1:c.256+2522T>G | ENSP00000470582.1:n.256+2522T>G | |
| ENST00000594187.1:n.132T>G | ||
| ENST00000598834.1:n.450T>G | ||
| NM_000767.4:c.548T>G | NP_000758.1:p.Val183Gly | |
| XM_005258569.3:c.548T>G | XP_005258626.1:p.Val183Gly | |
| XM_006723050.2:c.548T>G | XP_006723113.1:p.Val183Gly | |
| XM_011526546.1:c.548T>G | XP_011524848.1:p.Val183Gly | |
| XM_011526547.1:c.548T>G | XP_011524849.1:p.Val183Gly | |
| XM_011526548.1:c.484+2522T>G | XP_011524850.1:n.484+2522T>G | |
| XM_011526549.1:c.-44T>G | XP_011524851.1:n.-44T>G | |
| XM_011526550.1:c.364+2522T>G | XP_011524852.1:n.364+2522T>G | |
| NM_000767.5:c.548T>G MANE Select | NP_000758.1:p.Val183Gly |