HGVS | Genome Assembly |
---|---|
NC_000007.14:g.129213140del , CM000669.2:g.129213140del | GRCh38 |
NC_000007.13:g.128852981del , CM000669.1:g.128852981del | GRCh37 |
NC_000007.12:g.128640217del | NCBI36 |
NG_023340.1:g.29269del | |
NG_023340.2:g.29269del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000249373.8:c.*689del MANE Select | ENSP00000249373.3:n.*689del | |
ENST00000655644.1:c.*2808del | ENSP00000499377.1:n.*2808del | |
ENST00000249373.7:c.*689del | ENSP00000249373.3:n.*689del | |
NM_005631.4:c.*689del | NP_005622.1:n.*689del | |
XM_011516522.1:c.*689del | XP_011514824.1:n.*689del | |
XM_024446891.1:c.*689del | XP_024302659.1:n.*689del | |
NM_005631.5:c.*689del MANE Select | NP_005622.1:n.*689del |