Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.119341539G>C , CM000673.2:g.119341539G>C | GRCh38 |
| NC_000011.9:g.119212249G>C , CM000673.1:g.119212249G>C | GRCh37 |
| NC_000011.8:g.118717459G>C | NCBI36 |
| NG_012235.1:g.10135C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000619721.6:c.*9C>G (MFRP) MANE Select | ENSP00000481824.1:n.*9C>G | |
| ENST00000360167.4:c.*9C>G (MFRP) | ENSP00000353291.4:n.*9C>G | |
| ENST00000619721.5:c.*9C>G (MFRP) | ENSP00000481824.1:n.*9C>G | |
| NM_015645.4:c.-888C>G (C1QTNF5) | NP_056460.1:n.-888C>G | |
| NM_031433.3:c.*9C>G (MFRP) | NP_113621.1:n.*9C>G | |
| NM_031433.4:c.*9C>G (MFRP) MANE Select | NP_113621.1:n.*9C>G | |
| NM_015645.5:c.-888C>G (C1QTNF5) | NP_056460.1:n.-888C>G |