HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94782257_94782260del , CM000672.2:g.94782257_94782260del | GRCh38 |
NC_000010.10:g.96542014_96542017del , CM000672.1:g.96542014_96542017del | GRCh37 |
NC_000010.9:g.96532004_96532007del | NCBI36 |
NG_008384.2:g.24552_24555del | |
NG_008384.3:g.24577_24580del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.819+260_819+263del MANE Select | ENSP00000360372.3:n.819+260_819+263del | |
ENST00000645461.1:n.1872+260_1872+263del | ||
ENST00000371321.7:c.819+260_819+263del | ENSP00000360372.3:n.819+260_819+263del | |
ENST00000464755.1:c.1582+260_1582+263del | ENSP00000483243.1:n.1582+260_1582+263del | |
NM_000769.2:c.819+260_819+263del | NP_000760.1:n.819+260_819+263del | |
NM_000769.4:c.819+260_819+263del MANE Select | NP_000760.1:n.819+260_819+263del |