HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94782175_94782176delinsTG , CM000672.2:g.94782175_94782176delinsTG | GRCh38 |
NC_000010.10:g.96541932_96541933delinsTG , CM000672.1:g.96541932_96541933delinsTG | GRCh37 |
NC_000010.9:g.96531922_96531923delinsTG | NCBI36 |
NG_008384.2:g.24470_24471delinsTG | |
NG_008384.3:g.24495_24496delinsTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.819+178_819+179delinsTG MANE Select | ENSP00000360372.3:n.819+178_819+179delinsTG | |
ENST00000645461.1:n.1872+178_1872+179delinsTG | ||
ENST00000371321.7:c.819+178_819+179delinsTG | ENSP00000360372.3:n.819+178_819+179delinsTG | |
ENST00000464755.1:c.1582+178_1582+179delinsTG | ENSP00000483243.1:n.1582+178_1582+179delinsTG | |
NM_000769.2:c.819+178_819+179delinsTG | NP_000760.1:n.819+178_819+179delinsTG | |
NM_000769.4:c.819+178_819+179delinsTG MANE Select | NP_000760.1:n.819+178_819+179delinsTG |