Revel Score:
ENST00000257555 (MANE Select)
0.667
ENST00000535125
0.667
ENST00000543536
0.667
ENST00000544680
0.667
ENST00000537424
0.667
ENST00000543027
0.667
ENST00000545458
0.667
ENST00000541395
0.667
ENST00000340577
0.667
ENST00000344370
0.667
ENST00000544413
0.667
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.120979061C>G , CM000674.2:g.120979061C>G | GRCh38 |
| NC_000012.11:g.121416864C>G , CM000674.1:g.121416864C>G | GRCh37 |
| NC_000012.10:g.119901247C>G | NCBI36 |
| NG_011731.2:g.5316C>G , LRG_522:g.5316C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000560968.6:c.293C>G | ENSP00000453965.2:p.Ala98Gly | |
| ENST00000257555.11:c.293C>G MANE Select | ENSP00000257555.5:p.Ala98Gly | |
| ENST00000257555.10:c.293C>G | ENSP00000257555.4:p.Ala98Gly | |
| ENST00000400024.6:c.293C>G | ENSP00000476181.1:p.Ala98Gly | |
| ENST00000402929.5:n.428C>G | ||
| ENST00000535955.5:n.42+369C>G | ||
| ENST00000538626.2:n.190+221C>G | ||
| ENST00000538646.5:c.293C>G | ENSP00000443964.1:p.Ala98Gly | |
| ENST00000540108.1:c.293C>G | ENSP00000445445.1:p.Ala98Gly | |
| ENST00000541395.5:c.293C>G | ENSP00000443112.1:p.Ala98Gly | |
| ENST00000541924.5:c.293C>G | ENSP00000440361.1:p.Ala98Gly | |
| ENST00000543427.5:c.293C>G | ENSP00000439721.2:p.Ala98Gly | |
| ENST00000544413.2:c.293C>G | ENSP00000438804.1:p.Ala98Gly | |
| ENST00000544574.5:c.72+221C>G | ENSP00000438565.1:n.72+221C>G | |
| ENST00000560968.5:c.436C>G | ||
| ENST00000615446.4:c.-258+350C>G | ENSP00000483994.1:n.-258+350C>G | |
| ENST00000617366.4:c.293C>G | ENSP00000481967.1:p.Ala98Gly | |
| NM_000545.5:c.293C>G , LRG_522t1:c.293C>G | NP_000536.5:p.Ala98Gly | |
| NM_000545.6:c.293C>G | NP_000536.5:p.Ala98Gly | |
| NM_001306179.1:c.293C>G | NP_001293108.1:p.Ala98Gly | |
| XM_005253931.2:c.293C>G | XP_005253988.1:p.Ala98Gly | |
| XM_024449168.1:c.293C>G | XP_024304936.1:p.Ala98Gly | |
| NM_000545.8:c.293C>G MANE Select | NP_000536.6:p.Ala98Gly | |
| NM_001306179.2:c.293C>G | NP_001293108.2:p.Ala98Gly |