HGVS | Genome Assembly |
---|---|
NC_000012.12:g.91107216_91107217insAACAAAGA , CM000674.2:g.91107216_91107217insAACAAAGA | GRCh38 |
NC_000012.11:g.91500993_91500994insAACAAAGA , CM000674.1:g.91500993_91500994insAACAAAGA | GRCh37 |
NC_000012.10:g.90025124_90025125insAACAAAGA | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266718.5:c.862+906_862+907insGTTTCTTT MANE Select | ENSP00000266718.4:n.862+906_862+907insGTTTCTTT | |
ENST00000266718.4:c.862+906_862+907insGTTTCTTT | ENSP00000266718.4:n.862+906_862+907insGTTTCTTT | |
ENST00000546642.1:n.612+906_612+907insGTTTCTTT | ||
ENST00000548071.1:n.255+906_255+907insGTTTCTTT | ||
NM_002345.3:c.862+906_862+907insGTTTCTTT | NP_002336.1:n.862+906_862+907insGTTTCTTT | |
NM_002345.4:c.862+906_862+907insGTTTCTTT MANE Select | NP_002336.1:n.862+906_862+907insGTTTCTTT |