Revel Score:
ENST00000446342
0.092
ENST00000372764 (MANE Select)
0.092
ENST00000372762
0.092
ENST00000372761
0.092
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.73913343T>A , CM000672.2:g.73913343T>A | GRCh38 |
| NC_000010.10:g.75673101T>A , CM000672.1:g.75673101T>A | GRCh37 |
| NC_000010.9:g.75343107T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372764.4:c.422T>A (PLAU) MANE Select | ENSP00000361850.3:p.Leu141Gln | |
| ENST00000372764.3:c.422T>A (PLAU) | ENSP00000361850.3:p.Leu141Gln | |
| ENST00000409178.5:n.269-268A>T (C10orf55) | ||
| ENST00000412307.3:c.-73-268A>T (C10orf55) | ENSP00000409225.2:n.-73-268A>T | |
| ENST00000446342.5:c.371T>A (PLAU) | ENSP00000388474.1:p.Leu124Gln | |
| ENST00000494287.1:n.497T>A (PLAU) | ||
| NM_001001791.2:c.-73-268A>T (C10orf55) | NP_001001791.2:n.-73-268A>T | |
| XM_011539866.1:c.422T>A (PLAU) | XP_011538168.1:p.Leu141Gln | |
| XM_011539867.1:c.164T>A (PLAU) | XP_011538169.1:p.Leu55Gln | |
| XM_011539866.2:c.422T>A (PLAU) | XP_011538168.1:p.Leu141Gln | |
| NM_001145031.3:c.371T>A (PLAU) | NP_001138503.2:p.Leu124Gln | |
| NM_001319191.2:c.164T>A (PLAU) | NP_001306120.2:p.Leu55Gln | |
| NM_002658.6:c.422T>A (PLAU) MANE Select | NP_002649.2:p.Leu141Gln | |
| NR_160937.1:n.320-268A>T (C10orf55) | ||
| NR_160938.1:n.269-268A>T (C10orf55) |