HGVS | Genome Assembly |
---|---|
NC_000016.10:g.81315053_81315058del , CM000678.2:g.81315053_81315058del | GRCh38 |
NC_000016.9:g.81348658_81348663del , CM000678.1:g.81348658_81348663del | GRCh37 |
NC_000016.8:g.79906159_79906164del | NCBI36 |
NG_009007.1:g.5088_5093del , LRG_242:g.5088_5093del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000648349.2:c.-61_-56del | ENSP00000498114.1:n.-61_-56del | |
ENST00000648994.2:c.-61_-56del MANE Select | ENSP00000497351.1:n.-61_-56del | |
ENST00000674788.1:n.65_70del | ||
ENST00000568107.2:c.-61_-56del | ENSP00000476795.1:n.-61_-56del | |
NM_022041.3:c.-61_-56del , LRG_242t1:c.-61_-56del | NP_071324.1:n.-61_-56del | |
XM_017023734.1:c.-585_-580del | XP_016879223.1:n.-585_-580del | |
NM_001377486.1:c.-585_-580del | NP_001364415.1:n.-585_-580del | |
NM_022041.4:c.-61_-56del MANE Select | NP_071324.1:n.-61_-56del |