Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.119341687A>C , CM000673.2:g.119341687A>C | GRCh38 |
| NC_000011.9:g.119212397A>C , CM000673.1:g.119212397A>C | GRCh37 |
| NC_000011.8:g.118717607A>C | NCBI36 |
| NG_012235.1:g.9987T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000619721.6:c.1601T>G (MFRP) MANE Select | ENSP00000481824.1:p.Val534Gly | |
| ENST00000360167.4:c.1247T>G (MFRP) | ENSP00000353291.4:p.Val416Gly | |
| ENST00000449574.7:c.472T>G (MFRP) | ||
| ENST00000619721.5:c.1601T>G (MFRP) | ENSP00000481824.1:p.Val534Gly | |
| NM_015645.4:c.-1036T>G (C1QTNF5) | NP_056460.1:n.-1036T>G | |
| NM_031433.3:c.1601T>G (MFRP) | NP_113621.1:p.Val534Gly | |
| NM_031433.4:c.1601T>G (MFRP) MANE Select | NP_113621.1:p.Val534Gly | |
| NM_015645.5:c.-1036T>G (C1QTNF5) | NP_056460.1:n.-1036T>G |