HGVS | Genome Assembly |
---|---|
NC_000016.10:g.81315044_81315046del , CM000678.2:g.81315044_81315046del | GRCh38 |
NC_000016.9:g.81348649_81348651del , CM000678.1:g.81348649_81348651del | GRCh37 |
NC_000016.8:g.79906150_79906152del | NCBI36 |
NG_009007.1:g.5079_5081del , LRG_242:g.5079_5081del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000648349.2:c.-70_-68del | ENSP00000498114.1:n.-70_-68del | |
ENST00000648994.2:c.-70_-68del MANE Select | ENSP00000497351.1:n.-70_-68del | |
ENST00000674788.1:n.56_58del | ||
ENST00000568107.2:c.-70_-68del | ENSP00000476795.1:n.-70_-68del | |
NM_022041.3:c.-70_-68del , LRG_242t1:c.-70_-68del | NP_071324.1:n.-70_-68del | |
XM_017023734.1:c.-594_-592del | XP_016879223.1:n.-594_-592del | |
NM_001377486.1:c.-594_-592del | NP_001364415.1:n.-594_-592del | |
NM_022041.4:c.-70_-68del MANE Select | NP_071324.1:n.-70_-68del |