HGVS | Genome Assembly |
---|---|
NC_000005.10:g.140114156_140114161del , CM000667.2:g.140114156_140114161del | GRCh38 |
NC_000005.9:g.139493741_139493746del , CM000667.1:g.139493741_139493746del | GRCh37 |
NC_000005.8:g.139473925_139473930del | NCBI36 |
NG_041813.1:g.5034_5039del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331327.5:c.-26_-21del MANE Select | ENSP00000332706.3:n.-26_-21del | |
ENST00000505703.2:c.-26_-21del | ENSP00000498560.1:n.-26_-21del | |
ENST00000651386.1:c.-26_-21del | ENSP00000499133.1:n.-26_-21del | |
ENST00000331327.4:c.-26_-21del | ENSP00000332706.3:n.-26_-21del | |
ENST00000502351.1:n.398_403del | ||
ENST00000505703.1:n.440_445del | ||
NM_005859.4:c.-26_-21del | NP_005850.1:n.-26_-21del | |
NM_005859.5:c.-26_-21del MANE Select | NP_005850.1:n.-26_-21del |