HGVS | Genome Assembly |
---|---|
NC_000011.10:g.69648127del , CM000673.2:g.69648127del | GRCh38 |
NC_000011.9:g.69462895del , CM000673.1:g.69462895del | GRCh37 |
NC_000011.8:g.69172076del | NCBI36 |
NG_007375.1:g.12023del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000227507.3:c.708del MANE Select | ENSP00000227507.2:p.Ile237SerfsTer? | |
ENST00000227507.2:c.708del | ENSP00000227507.2:p.Ile237SerfsTer? | |
ENST00000536559.1:c.*128del | ENSP00000438482.1:n.*128del | |
ENST00000542367.1:n.171del | ||
ENST00000545484.1:n.414del | ||
NM_053056.2:c.708del | NP_444284.1:p.Ile237SerfsTer? | |
XM_006718653.2:c.732del | XP_006718716.1:p.Ile245SerfsTer? | |
NM_053056.3:c.708del MANE Select | NP_444284.1:p.Ile237SerfsTer? |