HGVS | Genome Assembly |
---|---|
NC_000012.12:g.91107201_91107202insGAA , CM000674.2:g.91107201_91107202insGAA | GRCh38 |
NC_000012.11:g.91500978_91500979insGAA , CM000674.1:g.91500978_91500979insGAA | GRCh37 |
NC_000012.10:g.90025109_90025110insGAA | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000266718.5:c.862+918_862+919insCTT MANE Select | ENSP00000266718.4:n.862+918_862+919insCTT | |
ENST00000266718.4:c.862+918_862+919insCTT | ENSP00000266718.4:n.862+918_862+919insCTT | |
ENST00000546642.1:n.612+918_612+919insCTT | ||
ENST00000548071.1:n.255+918_255+919insCTT | ||
NM_002345.3:c.862+918_862+919insCTT | NP_002336.1:n.862+918_862+919insCTT | |
NM_002345.4:c.862+918_862+919insCTT MANE Select | NP_002336.1:n.862+918_862+919insCTT |