HGVS | Genome Assembly |
---|---|
NC_000008.11:g.37966142_37966154del , CM000670.2:g.37966142_37966154del | GRCh38 |
NC_000008.10:g.37823660_37823672del , CM000670.1:g.37823660_37823672del | GRCh37 |
NC_000008.9:g.37942817_37942829del | NCBI36 |
NG_011936.1:g.5514_5526del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000345060.5:c.317_329del MANE Select | ENSP00000343782.3:p.Gly106AlafsTer12 | |
ENST00000520341.2:n.445_457del | ||
ENST00000345060.4:c.317_329del | ENSP00000343782.3:p.Gly106AlafsTer12 | |
ENST00000614635.1:c.317_329del | ENSP00000480325.1:p.Gly106AlafsTer12 | |
NM_000025.2:c.317_329del | NP_000016.1:p.Gly106AlafsTer12 | |
NM_000025.3:c.317_329del MANE Select | NP_000016.1:p.Gly106AlafsTer12 |