Revel Score:
ENST00000255226 (MANE Select)
0.276
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.45682394G>C , CM000680.2:g.45682394G>C | GRCh38 |
| NC_000018.9:g.43262359G>C , CM000680.1:g.43262359G>C | GRCh37 |
| NC_000018.8:g.41516357G>C | NCBI36 |
| NG_011775.4:g.370G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000255226.11:c.2638G>C MANE Select | ENSP00000255226.5:p.Ala880Pro | |
| ENST00000255226.10:c.2638G>C | ENSP00000255226.5:p.Ala880Pro | |
| ENST00000586448.5:c.2638G>C | ENSP00000465953.1:p.Ala880Pro | |
| ENST00000589658.5:c.2638G>C | ENSP00000465349.2:p.Ala880Pro | |
| NM_001242692.1:c.2638G>C | NP_001229621.1:p.Ala880Pro | |
| NM_007163.3:c.2638G>C | NP_009094.3:p.Ala880Pro | |
| XM_011526216.1:c.2638G>C | XP_011524518.1:p.Ala880Pro | |
| XM_011526217.1:c.2503G>C | XP_011524519.1:p.Ala835Pro | |
| XM_017026016.2:c.2503G>C | XP_016881505.1:p.Ala835Pro | |
| XM_024451270.1:c.2638G>C | XP_024307038.1:p.Ala880Pro | |
| XM_024451271.1:c.2638G>C | XP_024307039.1:p.Ala880Pro | |
| XR_935423.2:n.872+10001C>G | ||
| NM_001242692.2:c.2638G>C | NP_001229621.1:p.Ala880Pro | |
| NM_001371319.1:c.2638G>C | NP_001358248.1:p.Ala880Pro | |
| NM_007163.4:c.2638G>C MANE Select | NP_009094.3:p.Ala880Pro |