HGVS | Genome Assembly |
---|---|
NC_000007.14:g.1234193_1234194delinsAT , CM000669.2:g.1234193_1234194delinsAT | GRCh38 |
NC_000007.13:g.1273829_1273830delinsAT , CM000669.1:g.1273829_1273830delinsAT | GRCh37 |
NC_000007.12:g.1240355_1240356delinsAT | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000316333.9:c.450+498_450+499delinsAT MANE Select | ENSP00000314480.8:n.450+498_450+499delins... | |
ENST00000316333.8:c.450+498_450+499delinsAT | ENSP00000314480.8:n.450+498_450+499delins... | |
NM_001080461.1:c.450+498_450+499delinsAT | NP_001073930.1:n.450+498_450+499delinsAT | |
NM_001080461.2:c.450+498_450+499delinsAT | NP_001073930.1:n.450+498_450+499delinsAT | |
NM_001080461.3:c.450+498_450+499delinsAT MANE Select | NP_001073930.1:n.450+498_450+499delinsAT |