HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94782262_94782263insA , CM000672.2:g.94782262_94782263insA | GRCh38 |
NC_000010.10:g.96542019_96542020insA , CM000672.1:g.96542019_96542020insA | GRCh37 |
NC_000010.9:g.96532009_96532010insA | NCBI36 |
NG_008384.2:g.24557_24558insA | |
NG_008384.3:g.24582_24583insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.819+265_819+266insA MANE Select | ENSP00000360372.3:n.819+265_819+266insA | |
ENST00000645461.1:n.1872+265_1872+266insA | ||
ENST00000371321.7:c.819+265_819+266insA | ENSP00000360372.3:n.819+265_819+266insA | |
ENST00000464755.1:c.1582+265_1582+266insA | ENSP00000483243.1:n.1582+265_1582+266insA | |
NM_000769.2:c.819+265_819+266insA | NP_000760.1:n.819+265_819+266insA | |
NM_000769.4:c.819+265_819+266insA MANE Select | NP_000760.1:n.819+265_819+266insA |