HGVS | Genome Assembly |
---|---|
NC_000007.14:g.129213126del , CM000669.2:g.129213126del | GRCh38 |
NC_000007.13:g.128852967del , CM000669.1:g.128852967del | GRCh37 |
NC_000007.12:g.128640203del | NCBI36 |
NG_023340.1:g.29255del | |
NG_023340.2:g.29255del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000249373.8:c.*675del MANE Select | ENSP00000249373.3:n.*675del | |
ENST00000655644.1:c.*2794del | ENSP00000499377.1:n.*2794del | |
ENST00000249373.7:c.*675del | ENSP00000249373.3:n.*675del | |
NM_005631.4:c.*675del | NP_005622.1:n.*675del | |
XM_011516522.1:c.*675del | XP_011514824.1:n.*675del | |
XM_024446891.1:c.*675del | XP_024302659.1:n.*675del | |
NM_005631.5:c.*675del MANE Select | NP_005622.1:n.*675del |