HGVS | Genome Assembly |
---|---|
NC_000012.12:g.91107042_91107043insTAATCCCA , CM000674.2:g.91107042_91107043insTAATCCCA | GRCh38 |
NC_000012.11:g.91500819_91500820insTAATCCCA , CM000674.1:g.91500819_91500820insTAATCCCA | GRCh37 |
NC_000012.10:g.90024950_90024951insTAATCCCA | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266718.5:c.862+1075_862+1076insTGGGATTA MANE Select | ENSP00000266718.4:n.862+1075_862+1076insTGGGATTA | |
ENST00000266718.4:c.862+1075_862+1076insTGGGATTA | ENSP00000266718.4:n.862+1075_862+1076insTGGGATTA | |
ENST00000546642.1:n.612+1075_612+1076insTGGGATTA | ||
ENST00000548071.1:n.255+1075_255+1076insTGGGATTA | ||
NM_002345.3:c.862+1075_862+1076insTGGGATTA | NP_002336.1:n.862+1075_862+1076insTGGGATTA | |
NM_002345.4:c.862+1075_862+1076insTGGGATTA MANE Select | NP_002336.1:n.862+1075_862+1076insTGGGATTA |