Revel Score:
ENST00000374736 (MANE Select)
0.949
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.104831027T>A , CM000671.2:g.104831027T>A | GRCh38 |
| NC_000009.11:g.107593308T>A , CM000671.1:g.107593308T>A | GRCh37 |
| NC_000009.10:g.106633129T>A | NCBI36 |
| NG_007981.1:g.102129A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374736.8:c.1790A>T MANE Select | ENSP00000363868.3:p.Gln597Leu | |
| ENST00000678995.1:c.1790A>T | ENSP00000504612.1:p.Gln597Leu | |
| ENST00000374736.7:c.1790A>T | ENSP00000363868.3:p.Gln597Leu | |
| NM_005502.3:c.1790A>T | NP_005493.2:p.Gln597Leu | |
| XM_005251773.1:c.1790A>T | XP_005251830.1:p.Gln597Leu | |
| XM_005251776.1:c.1610A>T | XP_005251833.1:p.Gln537Leu | |
| XM_011518339.1:c.1865A>T | XP_011516641.1:p.Gln622Leu | |
| XM_011518340.1:c.1865A>T | XP_011516642.1:p.Gln622Leu | |
| XM_011518341.1:c.1865A>T | XP_011516643.1:p.Gln622Leu | |
| XM_011518342.1:c.1427A>T | XP_011516644.1:p.Gln476Leu | |
| XM_011518343.1:c.1865A>T | XP_011516645.1:p.Gln622Leu | |
| XM_011518344.1:c.1865A>T | XP_011516646.1:p.Gln622Leu | |
| XM_005251773.3:c.1790A>T | XP_005251830.1:p.Gln597Leu | |
| XM_005251776.3:c.1610A>T | XP_005251833.1:p.Gln537Leu | |
| XM_011518339.3:c.1865A>T | XP_011516641.1:p.Gln622Leu | |
| XM_011518340.3:c.1865A>T | XP_011516642.1:p.Gln622Leu | |
| XM_011518341.3:c.1865A>T | XP_011516643.1:p.Gln622Leu | |
| XM_011518342.3:c.1427A>T | XP_011516644.1:p.Gln476Leu | |
| XM_011518344.2:c.1865A>T | XP_011516646.1:p.Gln622Leu | |
| XM_017014378.2:c.1865A>T | XP_016869867.1:p.Gln622Leu | |
| XM_017014379.2:c.1865A>T | XP_016869868.1:p.Gln622Leu | |
| XM_017014380.2:c.1865A>T | XP_016869869.1:p.Gln622Leu | |
| XM_017014381.2:c.1865A>T | XP_016869870.1:p.Gln622Leu | |
| XM_017014382.2:c.1727A>T | XP_016869871.1:p.Gln576Leu | |
| XR_001746223.1:n.2178A>T | ||
| NM_005502.4:c.1790A>T MANE Select | NP_005493.2:p.Gln597Leu |