HGVS | Genome Assembly |
---|---|
NC_000004.12:g.67740132_67740133delinsGT , CM000666.2:g.67740132_67740133delinsGT | GRCh38 |
NC_000004.11:g.68605850_68605851delinsGT , CM000666.1:g.68605850_68605851delinsGT | GRCh37 |
NC_000004.10:g.68288445_68288446delinsGT | NCBI36 |
NG_009293.1:g.20954_20955delinsAC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000226413.5:c.*347_*348delinsAC MANE Select | ENSP00000226413.5:n.*347_*348delinsAC | |
ENST00000226413.4:c.*347_*348delinsAC | ENSP00000226413.4:n.*347_*348delinsAC | |
NM_000406.2:c.*347_*348delinsAC | NP_000397.1:n.*347_*348delinsAC | |
NM_001012763.1:c.*456_*457delinsAC | NP_001012781.1:n.*456_*457delinsAC | |
NM_000406.3:c.*347_*348delinsAC MANE Select | NP_000397.1:n.*347_*348delinsAC | |
NM_001012763.2:c.*456_*457delinsAC | NP_001012781.1:n.*456_*457delinsAC |