HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42900835del , CM000679.2:g.42900835del | GRCh38 |
NC_000017.10:g.41052852del , CM000679.1:g.41052852del | GRCh37 |
NC_000017.9:g.38306378del | NCBI36 |
NG_011808.1:g.5038del , LRG_147:g.5038del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000253801.7:c.-42del MANE Select | ENSP00000253801.1:n.-42del | |
ENST00000253801.6:c.-42del | ENSP00000253801.1:n.-42del | |
ENST00000585489.1:c.-42del | ENSP00000466202.1:n.-42del | |
ENST00000588481.1:n.24del | ||
ENST00000592383.5:c.-42del | ENSP00000465958.1:n.-42del | |
NM_000151.3:c.-42del | NP_000142.2:n.-42del | |
NM_001270397.1:c.-42del | NP_001257326.1:n.-42del | |
NM_000151.4:c.-42del MANE Select | NP_000142.2:n.-42del | |
NM_001270397.2:c.-42del | NP_001257326.1:n.-42del |