Revel Score:
ENST00000264832 (MANE Select)
0.025
gnomAD v2:
gnomAD v4:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10274864A>G , CM000681.2:g.10274864A>G | GRCh38 |
| NC_000019.9:g.10385540A>G , CM000681.1:g.10385540A>G | GRCh37 |
| NC_000019.8:g.10246540A>G | NCBI36 |
| NG_012083.1:g.9024A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264832.8:c.167A>G (ICAM1) MANE Select | ENSP00000264832.2:p.Lys56Arg | |
| ENST00000264832.7:c.167A>G (ICAM1) | ENSP00000264832.2:p.Lys56Arg | |
| ENST00000423829.2:c.67+3638A>G (ICAM1) | ENSP00000413124.2:n.67+3638A>G | |
| ENST00000588645.1:c.167A>G (ICAM1) | ENSP00000465680.1:p.Lys56Arg | |
| NM_000201.2:c.167A>G (ICAM1) | NP_000192.2:p.Lys56Arg | |
| XR_936313.1:n.155-8070T>C (LIMASI) | ||
| XR_936314.1:n.155-8070T>C (LIMASI) | ||
| NM_000201.3:c.167A>G (ICAM1) MANE Select | NP_000192.2:p.Lys56Arg |