HGVS | Genome Assembly |
---|---|
NC_000005.10:g.136046015_136046016insGC , CM000667.2:g.136046015_136046016insGC | GRCh38 |
NC_000005.9:g.135381704_135381705insGC , CM000667.1:g.135381704_135381705insGC | GRCh37 |
NC_000005.8:g.135409603_135409604insGC | NCBI36 |
NG_012646.1:g.22121_22122insGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000442011.7:c.299-320_299-319insGC MANE Select | ENSP00000416330.2:n.299-320_299-319insGC | |
ENST00000442011.6:c.299-320_299-319insGC | ENSP00000416330.2:n.299-320_299-319insGC | |
ENST00000504185.5:n.456-320_456-319insGC | ||
ENST00000506699.5:n.364-320_364-319insGC | ||
ENST00000507018.5:c.216-320_216-319insGC | ||
ENST00000515433.1:n.271_272insGC | ||
NM_000358.2:c.299-320_299-319insGC | NP_000349.1:n.299-320_299-319insGC | |
NM_000358.3:c.299-320_299-319insGC MANE Select | NP_000349.1:n.299-320_299-319insGC |