HGVS | Genome Assembly |
---|---|
NC_000009.12:g.129813564_129813567del , CM000671.2:g.129813564_129813567del | GRCh38 |
NC_000009.11:g.132575843_132575846del , CM000671.1:g.132575843_132575846del | GRCh37 |
NC_000009.10:g.131615664_131615667del | NCBI36 |
NG_008049.1:g.15603_15606del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000351698.5:c.*412_*415del MANE Select | ENSP00000345719.4:n.*412_*415del | |
ENST00000651202.1:c.*679_*682del | ENSP00000498222.1:n.*679_*682del | |
ENST00000351698.4:c.*412_*415del | ENSP00000345719.4:n.*412_*415del | |
NM_000113.2:c.*412_*415del | NP_000104.1:n.*412_*415del | |
XR_929731.3:n.1606_1609del | ||
NM_000113.3:c.*412_*415del MANE Select | NP_000104.1:n.*412_*415del |