Revel Score:
ENST00000343801
0.467
ENST00000400886
0.467
ENST00000292303 (MANE Select)
0.467
ENST00000445772
0.467
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.46373386C>T , CM000665.2:g.46373386C>T | GRCh38 |
| NC_000003.11:g.46414877C>T , CM000665.1:g.46414877C>T | GRCh37 |
| NC_000003.10:g.46389881C>T | NCBI36 |
| NG_012637.1:g.8245C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000292303.5:c.484C>T (CCR5) MANE Select | ENSP00000292303.4:p.Pro162Ser | |
| ENST00000292303.4:c.484C>T (CCR5) | ENSP00000292303.4:p.Pro162Ser | |
| ENST00000445772.1:c.484C>T (CCR5) | ENSP00000404881.1:p.Pro162Ser | |
| NM_000579.3:c.484C>T (CCR5) | NP_000570.1:p.Pro162Ser | |
| NM_001100168.1:c.484C>T (CCR5) | NP_001093638.1:p.Pro162Ser | |
| NR_125406.1:n.392-1969G>A (CCR5AS) | ||
| NM_000579.4:c.484C>T (CCR5) | NP_000570.1:p.Pro162Ser | |
| NM_001100168.2:c.484C>T (CCR5) | NP_001093638.1:p.Pro162Ser | |
| NM_001394783.1:c.484C>T (CCR5) MANE Select | NP_001381712.1:p.Pro162Ser |