HGVS | Genome Assembly |
---|---|
NC_000020.11:g.45547411del , CM000682.2:g.45547411del | GRCh38 |
NC_000020.10:g.44176050del , CM000682.1:g.44176050del | GRCh37 |
NC_000020.9:g.43609464del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651288.1:c.-54del (EPPIN-WFDC6) | ENSP00000498632.1:n.-54del | |
ENST00000354280.8:c.-54del (EPPIN) | ENSP00000361746.3:n.-54del | |
ENST00000409554.1:c.-54del (EPPIN) | ENSP00000387153.1:n.-54del | |
ENST00000504988.1:c.-54del (EPPIN-WFDC6) | ENSP00000424176.1:n.-54del | |
NM_001198986.1:c.-54del (EPPIN-WFDC6) | NP_001185915.1:n.-54del | |
NM_001302861.1:c.-54del (EPPIN) | NP_001289790.1:n.-54del | |
NM_020398.3:c.-54del (EPPIN) | NP_065131.1:n.-54del |