HGVS | Genome Assembly |
---|---|
NC_000022.11:g.37710538_37710539delinsGA , CM000684.2:g.37710538_37710539delinsGA | GRCh38 |
NC_000022.10:g.38106545_38106546delinsGA , CM000684.1:g.38106545_38106546delinsGA | GRCh37 |
NC_000022.9:g.36436491_36436492delinsGA | NCBI36 |
NG_012857.1:g.18551_18552delinsGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000644935.1:c.226_227delinsGA MANE Select | ENSP00000496394.1:p.Asp76= | |
ENST00000344404.10:c.226_227delinsGA | ENSP00000340312.6:p.Asp76= | |
ENST00000406386.7:c.226_227delinsGA | ENSP00000384312.3:p.Asp76= | |
ENST00000455236.4:c.1183_1184delinsGA | ENSP00000477208.1:n.1183_1184delinsGA | |
ENST00000492485.5:n.362_363delinsGA | ||
NM_001039141.2:c.226_227delinsGA | NP_001034230.1:p.Asp76= | |
NM_001039141.3:c.226_227delinsGA MANE Select | NP_001034230.1:p.Asp76= |