HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186199094del , CM000666.2:g.186199094del | GRCh38 |
NC_000004.11:g.187120248del , CM000666.1:g.187120248del | GRCh37 |
NC_000004.10:g.187357242del | NCBI36 |
NG_007965.1:g.12575del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378802.5:c.801+11del MANE Select | ENSP00000368079.4:n.801+11del | |
ENST00000378802.4:c.801+11del | ENSP00000368079.4:n.801+11del | |
ENST00000507209.5:n.1642+11del | ||
NM_207352.3:c.801+11del | NP_997235.3:n.801+11del | |
XM_005262935.2:c.801+11del | XP_005262992.1:n.801+11del | |
XM_006714184.2:c.405+11del | XP_006714247.1:n.405+11del | |
XM_005262935.4:c.801+11del | XP_005262992.1:n.801+11del | |
XM_017008037.1:c.405+11del | XP_016863526.1:n.405+11del | |
NM_207352.4:c.801+11del MANE Select | NP_997235.3:n.801+11del |