Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.119344455C>A , CM000673.2:g.119344455C>A | GRCh38 |
| NC_000011.9:g.119215165C>A , CM000673.1:g.119215165C>A | GRCh37 |
| NC_000011.8:g.118720375C>A | NCBI36 |
| NG_012235.1:g.7219G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000619721.6:c.899-64G>T (MFRP) MANE Select | ENSP00000481824.1:n.899-64G>T | |
| ENST00000360167.4:c.898+177G>T (MFRP) | ENSP00000353291.4:n.898+177G>T | |
| ENST00000619721.5:c.899-64G>T (MFRP) | ENSP00000481824.1:n.899-64G>T | |
| NM_015645.4:c.-1738-64G>T (C1QTNF5) | NP_056460.1:n.-1738-64G>T | |
| NM_031433.3:c.899-64G>T (MFRP) | NP_113621.1:n.899-64G>T | |
| NM_031433.4:c.899-64G>T (MFRP) MANE Select | NP_113621.1:n.899-64G>T | |
| NM_015645.5:c.-1738-64G>T (C1QTNF5) | NP_056460.1:n.-1738-64G>T |