HGVS | Genome Assembly |
---|---|
NC_000001.11:g.15445805_15445820del , CM000663.2:g.15445805_15445820del | GRCh38 |
NC_000001.10:g.15772300_15772315del , CM000663.1:g.15772300_15772315del | GRCh37 |
NC_000001.9:g.15644887_15644902del | NCBI36 |
NG_009253.1:g.12363_12378del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375949.5:c.792+56_792+71del MANE Select | ENSP00000365116.4:n.792+56_792+71del | |
ENST00000375943.6:c.*246+56_*246+71del | ENSP00000365110.2:n.*246+56_*246+71del | |
ENST00000375949.4:c.792+56_792+71del | ENSP00000365116.4:n.792+56_792+71del | |
ENST00000483406.1:n.556+56_556+71del | ||
NM_007272.2:c.792+56_792+71del | NP_009203.2:n.792+56_792+71del | |
XM_011540550.1:c.646+56_646+71del | XP_011538852.1:n.646+56_646+71del | |
NM_007272.3:c.792+56_792+71del MANE Select | NP_009203.2:n.792+56_792+71del |