HGVS | Genome Assembly |
---|---|
NC_000006.12:g.24301950_24301951delinsTA , CM000668.2:g.24301950_24301951delinsTA | GRCh38 |
NC_000006.11:g.24302178_24302179delinsTA , CM000668.1:g.24302178_24302179delinsTA | GRCh37 |
NC_000006.10:g.24410157_24410158delinsTA | NCBI36 |
NG_012829.1:g.61102_61103delinsTA | |
NG_012829.2:g.86342_86343delinsTA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378454.8:c.425+17_425+18delinsTA MANE Select | ENSP00000367715.3:n.425+17_425+18delinsTA | |
ENST00000378454.7:c.425+17_425+18delinsTA | ENSP00000367715.3:n.425+17_425+18delinsTA | |
NM_001195610.1:c.425+17_425+18delinsTA | NP_001182539.1:n.425+17_425+18delinsTA | |
NM_016356.4:c.425+17_425+18delinsTA | NP_057440.2:n.425+17_425+18delinsTA | |
NM_016356.5:c.425+17_425+18delinsTA MANE Select | NP_057440.2:n.425+17_425+18delinsTA | |
NM_001195610.2:c.425+17_425+18delinsTA | NP_001182539.1:n.425+17_425+18delinsTA |