Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102779726T>C , CM000673.2:g.102779726T>C | GRCh38 |
| NC_000011.9:g.102650457T>C , CM000673.1:g.102650457T>C | GRCh37 |
| NC_000011.8:g.102155667T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000279441.9:c.125A>G (MMP10) MANE Select | ENSP00000279441.4:p.Tyr42Cys | |
| ENST00000279441.8:c.125A>G (MMP10) | ENSP00000279441.4:p.Tyr42Cys | |
| ENST00000371455.7:n.325-18298T>C (WTAPP1) | ||
| ENST00000539681.1:c.125A>G (MMP10) | ENSP00000441485.1:p.Tyr42Cys | |
| NM_002425.2:c.125A>G (MMP10) | NP_002416.1:p.Tyr42Cys | |
| NM_002425.3:c.125A>G (MMP10) MANE Select | NP_002416.1:p.Tyr42Cys |