Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.119344305C>T , CM000673.2:g.119344305C>T | GRCh38 |
| NC_000011.9:g.119215015C>T , CM000673.1:g.119215015C>T | GRCh37 |
| NC_000011.8:g.118720225C>T | NCBI36 |
| NG_012235.1:g.7369G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000619721.6:c.975+10G>A (MFRP) MANE Select | ENSP00000481824.1:n.975+10G>A | |
| ENST00000360167.4:c.898+327G>A (MFRP) | ENSP00000353291.4:n.898+327G>A | |
| ENST00000619721.5:c.975+10G>A (MFRP) | ENSP00000481824.1:n.975+10G>A | |
| NM_015645.4:c.-1662+10G>A (C1QTNF5) | NP_056460.1:n.-1662+10G>A | |
| NM_031433.3:c.975+10G>A (MFRP) | NP_113621.1:n.975+10G>A | |
| NM_031433.4:c.975+10G>A (MFRP) MANE Select | NP_113621.1:n.975+10G>A | |
| NM_015645.5:c.-1662+10G>A (C1QTNF5) | NP_056460.1:n.-1662+10G>A |