Revel Score:
ENST00000378802 (MANE Select)
0.631
ENST00000274118
0.631
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186209173C>T , CM000666.2:g.186209173C>T | GRCh38 |
| NC_000004.11:g.187130327C>T , CM000666.1:g.187130327C>T | GRCh37 |
| NC_000004.10:g.187367321C>T | NCBI36 |
| NG_007965.1:g.22654C>T | |
| NG_012095.2:g.5195C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378802.5:c.1306C>T (CYP4V2) MANE Select | ENSP00000368079.4:p.Pro436Ser | |
| ENST00000378802.4:c.1306C>T (CYP4V2) | ENSP00000368079.4:p.Pro436Ser | |
| ENST00000502665.1:n.541C>T (CYP4V2) | ||
| ENST00000507209.5:n.6004C>T (CYP4V2) | ||
| ENST00000511608.5:c.102C>T (KLKB1) | ||
| ENST00000513354.5:n.396C>T (CYP4V2) | ||
| NM_207352.3:c.1306C>T (CYP4V2) | NP_997235.3:p.Pro436Ser | |
| XM_005262935.2:c.1303C>T (CYP4V2) | XP_005262992.1:p.Pro435Ser | |
| XM_006714184.2:c.910C>T (CYP4V2) | XP_006714247.1:p.Pro304Ser | |
| XM_005262935.4:c.1303C>T (CYP4V2) | XP_005262992.1:p.Pro435Ser | |
| XM_017008037.1:c.910C>T (CYP4V2) | XP_016863526.1:p.Pro304Ser | |
| NM_207352.4:c.1306C>T (CYP4V2) MANE Select | NP_997235.3:p.Pro436Ser |