HGVS | Genome Assembly |
---|---|
NC_000007.14:g.20164340_20164344delinsCTTGA , CM000669.2:g.20164340_20164344delinsCTTGA | GRCh38 |
NC_000007.13:g.20203963_20203967delinsCTTGA , CM000669.1:g.20203963_20203967delinsCTTGA | GRCh37 |
NC_000007.12:g.20170488_20170492delinsCTTGA | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000400331.10:c.-97_-93delinsTCAAG MANE Select | ENSP00000383185.3:n.-97_-93delinsTCAAG | |
ENST00000332878.8:c.-8-2474_-8-2470delinsTCAAG | ENSP00000328410.4:n.-8-2474_-8-2470delinsTCAAG | |
ENST00000400331.9:c.-97_-93delinsTCAAG | ENSP00000383185.3:n.-97_-93delinsTCAAG | |
ENST00000589011.1:c.-8-2474_-8-2470delinsTCAAG | ENSP00000466864.1:n.-8-2474_-8-2470delinsTCAAG | |
NM_182762.3:c.-97_-93delinsTCAAG | NP_877439.3:n.-97_-93delinsTCAAG | |
NM_182762.4:c.-97_-93delinsTCAAG MANE Select | NP_877439.3:n.-97_-93delinsTCAAG |