HGVS | Genome Assembly |
---|---|
NC_000007.14:g.107715990_107715994del , CM000669.2:g.107715990_107715994del | GRCh38 |
NC_000007.13:g.107356435_107356439del , CM000669.1:g.107356435_107356439del | GRCh37 |
NC_000007.12:g.107143671_107143675del | NCBI36 |
NG_008489.1:g.60356_60360del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000644269.2:c.*544_*548del MANE Select | ENSP00000494017.1:n.*544_*548del | |
ENST00000644846.1:c.1543_1547del | ||
ENST00000265715.7:c.*544_*548del | ENSP00000265715.3:n.*544_*548del | |
NM_000441.1:c.*544_*548del | NP_000432.1:n.*544_*548del | |
XM_005250425.2:c.*544_*548del | XP_005250482.1:n.*544_*548del | |
XM_017012318.1:c.*544_*548del | XP_016867807.1:n.*544_*548del | |
NM_000441.2:c.*544_*548del MANE Select | NP_000432.1:n.*544_*548del |