HGVS | Genome Assembly |
---|---|
NC_000021.9:g.43416924_43416946del , CM000683.2:g.43416924_43416946del | GRCh38 |
NG_052009.1:g.15193_15215del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270162.8:c.2154_2176del MANE Select | ENSP00000270162.6:p.Ser719AlafsTer? | |
ENST00000270162.6:c.2154_2176del | ENSP00000270162.6:p.Ser719AlafsTer? | |
NM_173354.3:c.2154_2176del | NP_775490.2:p.Ser719AlafsTer? | |
XM_011529474.1:c.2007_2029del | XP_011527776.1:p.Ser670AlafsTer? | |
NM_173354.4:c.2154_2176del | NP_775490.2:p.Ser719AlafsTer? | |
XM_011529474.2:c.2007_2029del | XP_011527776.1:p.Ser670AlafsTer? | |
NM_173354.5:c.2154_2176del MANE Select | NP_775490.2:p.Ser719AlafsTer? |