HGVS | Genome Assembly |
---|---|
NC_000001.11:g.15445834_15445853del , CM000663.2:g.15445834_15445853del | GRCh38 |
NC_000001.10:g.15772329_15772348del , CM000663.1:g.15772329_15772348del | GRCh37 |
NC_000001.9:g.15644916_15644935del | NCBI36 |
NG_009253.1:g.12392_12411del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375949.5:c.792+85_792+104del MANE Select | ENSP00000365116.4:n.792+85_792+104del | |
ENST00000375943.6:c.*246+85_*246+104del | ENSP00000365110.2:n.*246+85_*246+104del | |
ENST00000375949.4:c.792+85_792+104del | ENSP00000365116.4:n.792+85_792+104del | |
ENST00000483406.1:n.556+85_556+104del | ||
NM_007272.2:c.792+85_792+104del | NP_009203.2:n.792+85_792+104del | |
XM_011540550.1:c.646+85_646+104del | XP_011538852.1:n.646+85_646+104del | |
NM_007272.3:c.792+85_792+104del MANE Select | NP_009203.2:n.792+85_792+104del |