HGVS | Genome Assembly |
---|---|
NC_000023.11:g.78123052_78123053delinsTC , CM000685.2:g.78123052_78123053delinsTC | GRCh38 |
NC_000023.10:g.77378549_77378550delinsTC , CM000685.1:g.77378549_77378550delinsTC | GRCh37 |
NC_000023.9:g.77265205_77265206delinsTC | NCBI36 |
NG_008862.1:g.23884_23885delinsTC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373316.5:c.756+103_756+104delinsTC MANE Select | ENSP00000362413.4:n.756+103_756+104delinsTC | |
ENST00000644362.1:c.672+103_672+104delinsTC | ENSP00000496140.1:n.672+103_672+104delinsTC | |
ENST00000373316.4:c.756+103_756+104delinsTC | ENSP00000362413.4:n.756+103_756+104delinsTC | |
ENST00000474281.1:n.163+51_163+52delinsTC | ||
NM_000291.3:c.756+103_756+104delinsTC | NP_000282.1:n.756+103_756+104delinsTC | |
NM_000291.4:c.756+103_756+104delinsTC MANE Select | NP_000282.1:n.756+103_756+104delinsTC |