HGVS | Genome Assembly |
---|---|
NC_000002.12:g.96143595_96143596insGTAGA , CM000664.2:g.96143595_96143596insGTAGA | GRCh38 |
NC_000002.11:g.96809334_96809335insGTAGA , CM000664.1:g.96809334_96809335insGTAGA | GRCh37 |
NC_000002.10:g.96173061_96173062insGTAGA | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000288943.5:c.*227_*228insTCTAC MANE Select | ENSP00000288943.4:n.*227_*228insTCTAC | |
ENST00000288943.4:c.*227_*228insTCTAC | ENSP00000288943.4:n.*227_*228insTCTAC | |
NM_004418.3:c.*227_*228insTCTAC | NP_004409.1:n.*227_*228insTCTAC | |
XM_017003546.1:c.*227_*228insTCTAC | XP_016859035.1:n.*227_*228insTCTAC | |
NM_004418.4:c.*227_*228insTCTAC MANE Select | NP_004409.1:n.*227_*228insTCTAC |