HGVS | Genome Assembly |
---|---|
NC_000002.12:g.43887164_43887167delinsAGAT , CM000664.2:g.43887164_43887167delinsAGAT | GRCh38 |
NC_000002.11:g.44114303_44114306delinsAGAT , CM000664.1:g.44114303_44114306delinsAGAT | GRCh37 |
NC_000002.10:g.43967807_43967810delinsAGAT | NCBI36 |
NG_008247.1:g.113839_113842delinsATCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682612.1:c.2385_2388delinsATCT | ||
ENST00000684454.1:n.9482_9485delinsATCT | ||
ENST00000260665.12:c.*1433_*1436delinsATCT MANE Select | ENSP00000260665.7:n.*1433_*1436delinsATCT | |
ENST00000260665.11:c.*1433_*1436delinsATCT | ENSP00000260665.7:n.*1433_*1436delinsATCT | |
NM_133259.3:c.*1433_*1436delinsATCT | NP_573566.2:n.*1433_*1436delinsATCT | |
XR_002958896.1:n.5800_5803delinsATCT | ||
NM_133259.4:c.*1433_*1436delinsATCT MANE Select | NP_573566.2:n.*1433_*1436delinsATCT |