HGVS | Genome Assembly |
---|---|
NC_000007.14:g.27095418_27095419delinsTC , CM000669.2:g.27095418_27095419delinsTC | GRCh38 |
NC_000007.13:g.27135037_27135038delinsTC , CM000669.1:g.27135037_27135038delinsTC | GRCh37 |
NC_000007.12:g.27101562_27101563delinsTC | NCBI36 |
NG_011813.1:g.5588_5589delinsGA | |
NG_033087.1:g.4325_4326delinsTC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000643460.2:c.494_495delinsGA MANE Select | ENSP00000494260.2:p.Gly165= | |
ENST00000343060.4:c.494_495delinsGA | ENSP00000343246.4:p.Gly165= | |
ENST00000355633.5:c.355-64_355-63delinsGA | ENSP00000347851.5:n.355-64_355-63delinsGA | |
NM_005522.4:c.494_495delinsGA | NP_005513.1:p.Gly165= | |
NM_153620.2:c.355-64_355-63delinsGA | NP_705873.2:n.355-64_355-63delinsGA | |
NM_005522.5:c.494_495delinsGA MANE Select | NP_005513.2:p.Gly165= | |
NM_153620.3:c.355-64_355-63delinsGA | NP_705873.3:n.355-64_355-63delinsGA |