HGVS | Genome Assembly |
---|---|
NC_000002.12:g.167954910del , CM000664.2:g.167954910del | GRCh38 |
NC_000002.11:g.168811420del , CM000664.1:g.168811420del | GRCh37 |
NC_000002.10:g.168519666del | NCBI36 |
NG_052783.1:g.297692del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000697205.1:c.2167del | ENSP00000513185.1:n.2167del | |
ENST00000355999.5:c.*592del MANE Select | ENSP00000348278.4:n.*592del | |
ENST00000355999.4:c.*592del | ENSP00000348278.4:n.*592del | |
ENST00000487143.5:n.1330del | ||
NM_013233.2:c.*592del | NP_037365.2:n.*592del | |
XM_005246465.2:c.*592del | XP_005246522.1:n.*592del | |
XM_011510966.1:c.*592del | XP_011509268.1:n.*592del | |
XM_011510967.1:c.*592del | XP_011509269.1:n.*592del | |
NM_013233.3:c.*592del MANE Select | NP_037365.2:n.*592del |