HGVS | Genome Assembly |
---|---|
NC_000011.10:g.89178663del , CM000673.2:g.89178663del | GRCh38 |
NC_000011.9:g.88911831del , CM000673.1:g.88911831del | GRCh37 |
NC_000011.8:g.88551479del | NCBI36 |
NG_008748.1:g.5792del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263321.6:c.710del MANE Select | ENSP00000263321.4:p.Asp237AlafsTer? | |
ENST00000263321.5:c.710del | ENSP00000263321.4:p.Asp237AlafsTer? | |
ENST00000526139.1:n.771del | ||
NM_000372.4:c.710del | NP_000363.1:p.Asp237AlafsTer? | |
XM_011542970.1:c.710del | XP_011541272.1:p.Asp237AlafsTer? | |
XM_011542970.2:c.710del | XP_011541272.1:p.Asp237AlafsTer? | |
XR_001748321.1:n.2718-65130del | ||
XR_001748322.1:n.2733-65130del | ||
NM_000372.5:c.710del MANE Select | NP_000363.1:p.Asp237AlafsTer? |