HGVS | Genome Assembly |
---|---|
NC_000017.11:g.82727661_82727664del , CM000679.2:g.82727661_82727664del | GRCh38 |
NC_000017.10:g.80685537_80685540del , CM000679.1:g.80685537_80685540del | GRCh37 |
NC_000017.9:g.78278826_78278829del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000269373.11:c.*490_*493del MANE Select | ENSP00000269373.6:n.*490_*493del | |
ENST00000269373.10:c.*490_*493del | ENSP00000269373.6:n.*490_*493del | |
ENST00000571594.1:c.53+494_53+497del | ENSP00000459751.1:n.53+494_53+497del | |
NM_024619.3:c.*490_*493del | NP_078895.2:n.*490_*493del | |
NR_046408.1:n.1598_1601del | ||
XM_024450948.1:c.*490_*493del | XP_024306716.1:n.*490_*493del | |
NM_024619.4:c.*490_*493del MANE Select | NP_078895.2:n.*490_*493del | |
NR_046408.2:n.1598_1601del |