HGVS | Genome Assembly |
---|---|
NC_000016.10:g.81315026_81315027insT , CM000678.2:g.81315026_81315027insT | GRCh38 |
NC_000016.9:g.81348631_81348632insT , CM000678.1:g.81348631_81348632insT | GRCh37 |
NC_000016.8:g.79906132_79906133insT | NCBI36 |
NG_009007.1:g.5061_5062insT , LRG_242:g.5061_5062insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000648349.2:c.-88_-87insT | ENSP00000498114.1:n.-88_-87insT | |
ENST00000648994.2:c.-88_-87insT MANE Select | ENSP00000497351.1:n.-88_-87insT | |
ENST00000674788.1:n.38_39insT | ||
ENST00000568107.2:c.-88_-87insT | ENSP00000476795.1:n.-88_-87insT | |
NM_022041.3:c.-88_-87insT , LRG_242t1:c.-88_-87insT | NP_071324.1:n.-88_-87insT | |
XM_017023734.1:c.-612_-611insT | XP_016879223.1:n.-612_-611insT | |
NM_001377486.1:c.-612_-611insT | NP_001364415.1:n.-612_-611insT | |
NM_022041.4:c.-88_-87insT MANE Select | NP_071324.1:n.-88_-87insT |