HGVS | Genome Assembly |
---|---|
NC_000016.10:g.81315034_81315040del , CM000678.2:g.81315034_81315040del | GRCh38 |
NC_000016.9:g.81348639_81348645del , CM000678.1:g.81348639_81348645del | GRCh37 |
NC_000016.8:g.79906140_79906146del | NCBI36 |
NG_009007.1:g.5069_5075del , LRG_242:g.5069_5075del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000648349.2:c.-80_-74del | ENSP00000498114.1:n.-80_-74del | |
ENST00000648994.2:c.-80_-74del MANE Select | ENSP00000497351.1:n.-80_-74del | |
ENST00000674788.1:n.46_52del | ||
ENST00000568107.2:c.-80_-74del | ENSP00000476795.1:n.-80_-74del | |
NM_022041.3:c.-80_-74del , LRG_242t1:c.-80_-74del | NP_071324.1:n.-80_-74del | |
XM_017023734.1:c.-604_-598del | XP_016879223.1:n.-604_-598del | |
NM_001377486.1:c.-604_-598del | NP_001364415.1:n.-604_-598del | |
NM_022041.4:c.-80_-74del MANE Select | NP_071324.1:n.-80_-74del |