HGVS | Genome Assembly |
---|---|
NC_000004.12:g.67932032del , CM000666.2:g.67932032del | GRCh38 |
NC_000004.11:g.68797750del , CM000666.1:g.68797750del | GRCh37 |
NC_000004.10:g.68480345del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000508048.6:c.282del MANE Select | ENSP00000426911.2:p.Trp94Ter | |
ENST00000334830.11:c.291del | ENSP00000334611.7:p.Trp97Ter | |
ENST00000396188.3:c.282del | ENSP00000379491.3:p.Trp94Ter | |
ENST00000508048.5:c.282del | ENSP00000426911.2:p.Trp94Ter | |
ENST00000513536.5:c.222del | ENSP00000427621.1:p.Trp74Ter | |
NM_001114387.1:c.282del | NP_001107859.1:p.Trp94Ter | |
NM_182606.3:c.291del | NP_872412.3:p.Trp97Ter | |
NM_001114387.2:c.282del MANE Select | NP_001107859.1:p.Trp94Ter | |
NM_182606.4:c.291del | NP_872412.3:p.Trp97Ter |