HGVS | Genome Assembly |
---|---|
NC_000023.11:g.78123079_78123080insA , CM000685.2:g.78123079_78123080insA | GRCh38 |
NC_000023.10:g.77378576_77378577insA , CM000685.1:g.77378576_77378577insA | GRCh37 |
NC_000023.9:g.77265232_77265233insA | NCBI36 |
NG_008862.1:g.23911_23912insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373316.5:c.757-116_757-115insA MANE Select | ENSP00000362413.4:n.757-116_757-115insA | |
ENST00000644362.1:c.673-116_673-115insA | ENSP00000496140.1:n.673-116_673-115insA | |
ENST00000373316.4:c.757-116_757-115insA | ENSP00000362413.4:n.757-116_757-115insA | |
ENST00000474281.1:n.163+78_163+79insA | ||
NM_000291.3:c.757-116_757-115insA | NP_000282.1:n.757-116_757-115insA | |
NM_000291.4:c.757-116_757-115insA MANE Select | NP_000282.1:n.757-116_757-115insA |