HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5226765_5226766delinsAG , CM000673.2:g.5226765_5226766delinsAG | GRCh38 |
NC_000011.9:g.5247995_5247996delinsAG , CM000673.1:g.5247995_5247996delinsAG | GRCh37 |
NC_000011.8:g.5204571_5204572delinsAG | NCBI36 |
NG_000007.3:g.70850_70851delinsCT | |
NG_059281.1:g.5306_5307delinsCT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647020.1:c.126_127delinsCT | ENSP00000494175.1:p.Phe42= | |
ENST00000335295.4:c.126_127delinsCT MANE Select | ENSP00000333994.3:p.Phe42= | |
ENST00000380315.2:c.126_127delinsCT | ENSP00000369671.2:p.Phe42= | |
ENST00000475226.1:n.58_59delinsCT | ||
ENST00000485743.1:n.177_178delinsCT | ||
ENST00000633227.1:c.110_111delinsCT | ENSP00000488004.1:p.Ser37= | |
NM_000518.4:c.126_127delinsCT | NP_000509.1:p.Phe42= | |
NM_000518.5:c.126_127delinsCT MANE Select | NP_000509.1:p.Phe42= |