HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31270325del , CM000668.2:g.31270325del | GRCh38 |
NC_000006.11:g.31238102del , CM000668.1:g.31238102del | GRCh37 |
NC_000006.10:g.31346081del | NCBI36 |
NG_029422.2:g.6807del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376228.10:c.780del MANE Select | ENSP00000365402.5:p.Gly261GlufsTer? | |
ENST00000376228.9:c.780del | ENSP00000365402.5:p.Gly261GlufsTer? | |
ENST00000376237.8:c.*367del | ENSP00000365412.4:n.*367del | |
ENST00000383329.7:c.780del | ENSP00000372819.3:p.Gly261GlufsTer? | |
ENST00000415537.1:c.671del | ||
ENST00000470363.5:n.98del | ||
ENST00000487245.5:n.1139del | ||
ENST00000495835.1:n.969del | ||
NM_002117.5:c.780del | NP_002108.4:p.Gly261GlufsTer? | |
NM_002117.6:c.780del MANE Select | NP_002108.4:p.Gly261GlufsTer? |