Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102772013A>C , CM000673.2:g.102772013A>C | GRCh38 |
| NC_000011.9:g.102642744A>C , CM000673.1:g.102642744A>C | GRCh37 |
| NC_000011.8:g.102147954A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000279441.9:c.1329T>G (MMP10) MANE Select | ENSP00000279441.4:p.Phe443Leu | |
| ENST00000279441.8:c.1329T>G (MMP10) | ENSP00000279441.4:p.Phe443Leu | |
| ENST00000371455.7:n.324+20587A>C (WTAPP1) | ||
| NM_002425.2:c.1329T>G (MMP10) | NP_002416.1:p.Phe443Leu | |
| NM_002425.3:c.1329T>G (MMP10) MANE Select | NP_002416.1:p.Phe443Leu |