HGVS | Genome Assembly |
---|---|
NC_000006.12:g.131851112_131851120del , CM000668.2:g.131851112_131851120del | GRCh38 |
NC_000006.11:g.132172252_132172260del , CM000668.1:g.132172252_132172260del | GRCh37 |
NC_000006.10:g.132213945_132213953del | NCBI36 |
NG_008206.1:g.48097_48105del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647893.1:c.431-30_431-22del MANE Select | ENSP00000498074.1:n.431-30_431-22del | |
ENST00000650147.1:c.109-30_109-22del | ||
ENST00000650437.1:c.108+1006_108+1014del | ||
ENST00000360971.6:c.431-30_431-22del | ENSP00000354238.2:n.431-30_431-22del | |
ENST00000486853.1:n.451-30_451-22del | ||
ENST00000513998.5:c.431-30_431-22del | ENSP00000422424.1:n.431-30_431-22del | |
NM_006208.2:c.431-30_431-22del | NP_006199.2:n.431-30_431-22del | |
NM_006208.3:c.431-30_431-22del MANE Select | NP_006199.2:n.431-30_431-22del |