HGVS | Genome Assembly |
---|---|
NC_000012.12:g.91107243_91107244insCAAG , CM000674.2:g.91107243_91107244insCAAG | GRCh38 |
NC_000012.11:g.91501020_91501021insCAAG , CM000674.1:g.91501020_91501021insCAAG | GRCh37 |
NC_000012.10:g.90025151_90025152insCAAG | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266718.5:c.862+877_862+878insGCTT MANE Select | ENSP00000266718.4:n.862+877_862+878insGCTT | |
ENST00000266718.4:c.862+877_862+878insGCTT | ENSP00000266718.4:n.862+877_862+878insGCTT | |
ENST00000546642.1:n.612+877_612+878insGCTT | ||
ENST00000548071.1:n.255+877_255+878insGCTT | ||
NM_002345.3:c.862+877_862+878insGCTT | NP_002336.1:n.862+877_862+878insGCTT | |
NM_002345.4:c.862+877_862+878insGCTT MANE Select | NP_002336.1:n.862+877_862+878insGCTT |