Revel Score:
ENST00000225964 (MANE Select)
0.397
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00001747 (AFR)
Genomes Max Group AF
0.000008 (AFR)
Exomes Max Group AF
0.00000991 (AFR)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.50188923G>A , CM000679.2:g.50188923G>A | GRCh38 |
| NC_000017.10:g.48266284G>A , CM000679.1:g.48266284G>A | GRCh37 |
| NC_000017.9:g.45621283G>A | NCBI36 |
| NG_007400.1:g.17717C>T , LRG_1:g.17717C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225964.10:c.3025C>T MANE Select | ENSP00000225964.6:p.Pro1009Ser | |
| ENST00000225964.9:c.3025C>T | ENSP00000225964.5:p.Pro1009Ser | |
| NM_000088.3:c.3025C>T , LRG_1t1:c.3025C>T | NP_000079.2:p.Pro1009Ser | |
| XM_005257058.3:c.2755C>T | XP_005257115.2:p.Pro919Ser | |
| XM_005257059.3:c.2107C>T | XP_005257116.2:p.Pro703Ser | |
| XM_011524341.1:c.2827C>T | XP_011522643.1:p.Pro943Ser | |
| XM_005257058.4:c.2755C>T | XP_005257115.2:p.Pro919Ser | |
| XM_005257059.4:c.2107C>T | XP_005257116.2:p.Pro703Ser | |
| NM_000088.4:c.3025C>T MANE Select | NP_000079.2:p.Pro1009Ser |