HGVS | Genome Assembly |
---|---|
NC_000017.11:g.8075582_8075583delinsTC , CM000679.2:g.8075582_8075583delinsTC | GRCh38 |
NC_000017.10:g.7978900_7978901delinsTC , CM000679.1:g.7978900_7978901delinsTC | GRCh37 |
NC_000017.9:g.7919625_7919626delinsTC | NCBI36 |
NG_007099.1:g.17121_17122delinsGA | |
NG_007099.2:g.17134_17135delinsGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647874.1:c.1654+12_1654+13delinsGA MANE Select | ENSP00000497784.1:n.1654+12_1654+13delinsGA | |
ENST00000649809.1:c.718+12_718+13delinsGA | ENSP00000496845.1:n.718+12_718+13delinsGA | |
ENST00000319144.4:c.1654+12_1654+13delinsGA | ENSP00000315167.4:n.1654+12_1654+13delinsGA | |
ENST00000577351.5:n.479+592_479+593delinsGA | ||
NM_001139.2:c.1654+12_1654+13delinsGA | NP_001130.1:n.1654+12_1654+13delinsGA | |
NM_001139.3:c.1654+12_1654+13delinsGA MANE Select | NP_001130.1:n.1654+12_1654+13delinsGA |