HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5226678dup , CM000673.2:g.5226678dup | GRCh38 |
NC_000011.9:g.5247908dup , CM000673.1:g.5247908dup | GRCh37 |
NC_000011.8:g.5204484dup | NCBI36 |
NG_000007.3:g.70940dup | |
NG_059281.1:g.5396dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647020.1:c.216dup | ENSP00000494175.1:p.Ser73Ter | |
ENST00000335295.4:c.216dup MANE Select | ENSP00000333994.3:p.Ser73Ter | |
ENST00000380315.2:c.216dup | ENSP00000369671.2:p.Ser73Ter | |
ENST00000475226.1:n.148dup | ||
ENST00000485743.1:n.267dup | ||
ENST00000633227.1:c.*32dup | ENSP00000488004.1:n.*32dup | |
NM_000518.4:c.216dup | NP_000509.1:p.Ser73Ter | |
NM_000518.5:c.216dup MANE Select | NP_000509.1:p.Ser73Ter |