HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186199076_186199078del , CM000666.2:g.186199076_186199078del | GRCh38 |
NC_000004.11:g.187120230_187120232del , CM000666.1:g.187120230_187120232del | GRCh37 |
NC_000004.10:g.187357224_187357226del | NCBI36 |
NG_007965.1:g.12557_12559del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000378802.5:c.794_796del MANE Select | ENSP00000368079.4:p.Thr265del | |
ENST00000378802.4:c.794_796del | ENSP00000368079.4:p.Thr265del | |
ENST00000507209.5:n.1635_1637del | ||
NM_207352.3:c.794_796del | NP_997235.3:p.Thr265del | |
XM_005262935.2:c.794_796del | XP_005262992.1:p.Thr265del | |
XM_006714184.2:c.398_400del | XP_006714247.1:p.Thr133del | |
XM_005262935.4:c.794_796del | XP_005262992.1:p.Thr265del | |
XM_017008037.1:c.398_400del | XP_016863526.1:p.Thr133del | |
NM_207352.4:c.794_796del MANE Select | NP_997235.3:p.Thr265del |