HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1423570_1423578delinsTCGCAGTTC , CM000667.2:g.1423570_1423578delinsTCGCAGTTC | GRCh38 |
NC_000005.9:g.1423685_1423693delinsTCGCAGTTC , CM000667.1:g.1423685_1423693delinsTCGCAGTTC | GRCh37 |
NC_000005.8:g.1476685_1476693delinsTCGCAGTTC | NCBI36 |
NG_015885.1:g.26851_26859delinsGAACTGCGA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000270349.12:c.654-1564_654-1556delinsGAACTGCGA MANE Select | ENSP00000270349.9:n.654-1564_654-1556delinsGAACTGCGA | |
ENST00000270349.11:c.654-1564_654-1556delinsGAACTGCGA | ENSP00000270349.9:n.654-1564_654-1556delinsGAACTGCGA | |
NM_001044.4:c.654-1564_654-1556delinsGAACTGCGA | NP_001035.1:n.654-1564_654-1556delinsGAACTGCGA | |
NM_001044.5:c.654-1564_654-1556delinsGAACTGCGA MANE Select | NP_001035.1:n.654-1564_654-1556delinsGAACTGCGA |