HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5226733_5226734delinsAT , CM000673.2:g.5226733_5226734delinsAT | GRCh38 |
NC_000011.9:g.5247963_5247964delinsAT , CM000673.1:g.5247963_5247964delinsAT | GRCh37 |
NC_000011.8:g.5204539_5204540delinsAT | NCBI36 |
NG_000007.3:g.70882_70883delinsAT | |
NG_059281.1:g.5338_5339delinsAT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647020.1:c.158_159delinsAT | ENSP00000494175.1:p.Asp53= | |
ENST00000335295.4:c.158_159delinsAT MANE Select | ENSP00000333994.3:p.Asp53= | |
ENST00000380315.2:c.158_159delinsAT | ENSP00000369671.2:p.Asp53= | |
ENST00000475226.1:n.90_91delinsAT | ||
ENST00000485743.1:n.209_210delinsAT | ||
ENST00000633227.1:c.142_143delinsAT | ENSP00000488004.1:p.Met48= | |
NM_000518.4:c.158_159delinsAT | NP_000509.1:p.Asp53= | |
NM_000518.5:c.158_159delinsAT MANE Select | NP_000509.1:p.Asp53= |