HGVS | Genome Assembly |
---|---|
NC_000017.11:g.43755526_43755527delinsAT , CM000679.2:g.43755526_43755527delinsAT | GRCh38 |
NC_000017.10:g.41832894_41832895delinsAT , CM000679.1:g.41832894_41832895delinsAT | GRCh37 |
NC_000017.9:g.39188420_39188421delinsAT | NCBI36 |
NG_008078.2:g.8262_8263delinsAT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301691.3:c.457_458delinsAT MANE Select | ENSP00000301691.1:p.Ala153Met | |
ENST00000301691.2:c.457_458delinsAT | ENSP00000301691.1:p.Ala153Met | |
NM_025237.2:c.457_458delinsAT | NP_079513.1:p.Ala153Met | |
NM_025237.3:c.457_458delinsAT MANE Select | NP_079513.1:p.Ala153Met |